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EAEU HS code

3822 19 000 9 — Diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, whether or not put up in the form of kits, other than those of heading 3006; certified reference materials: diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, whether or not put up in the form of kits: other: other

Diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, whether or not put up in the form of kits: other: other

Full name

Diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, whether or not put up in the form of kits, other than those of heading 3006; certified reference materials: diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, whether or not put up in the form of kits: other: other

Names come in English where the EU Combined Nomenclature publishes them — chapters, headings and subheadings, whose first six digits are the same Harmonized System; deeper EAEU detail is a machine translation, marked as such. Official texts — tariff notes, measures, lists and classification rulings — are the original: customs and your broker go by that wording. Where we show a machine translation of them, it is marked; where our quality check rejected one, the Russian stays.

Machine translation. The original is the Russian text of the EAEU tariff, and customs goes by it; this translation is for understanding only and has no legal force.

Duty rate
5%

This is the base rate. A tariff quota, a preference for the country of origin and a tariff exemption lower it; anti-dumping and special duties are paid on top of it

EEC Council Decision No. 80 of 14.09.2021

Supplementary unit
Not applicable
Requirements and measures
5

None: mandatory labelling, recycling fee, export control, EAEU non-tariff regulation, trade defence measures — duty on top of the tariff, tariff quota.

Whether a measure applies to your goods depends on their characteristics and the shipping documents

VAT
VAT-exempt or 22%

Exempt if the goods match a description on exemption list No. 1042. Otherwise 22%.

Product reference in Word (in Russian)

Duties, taxes, fees, bans, permits and controls in one free file.

Import into Russia

Import reference

Export from Russia

Export reference

Import into Russia

Payments on import

Duty for this code: 5%. On top of the duty, on import into Russia you pay VAT of 22% (unless the goods are VAT-exempt) of the customs value including the duty (Article 160 of the Tax Code) and the customs processing fee — a fixed amount by value band. Customs value: the price of the goods, delivery to the border, local costs.

The CCT rate applies from Mar 8, 2026: Решение Совета ЕЭК № 13 от 30.01.2026.

How the rate for this code has changed
Customs fee scale by customs value, 2026
  • from 0 to 200,000 ₽1,231 ₽
  • from 200,000 to 450,000 ₽2,462 ₽
  • from 450,000 to 1,200,000 ₽4,924 ₽
  • from 1,200,000 to 2,700,000 ₽13,541 ₽
  • from 2,700,000 to 4,200,000 ₽18,465 ₽
  • from 4,200,000 to 5,500,000 ₽21,344 ₽
  • from 5,500,000 to 10,000,000 ₽49,240 ₽
  • over 10,000,000 ₽73,860 ₽

Fee per declaration. Russian Government Resolution No. 1637 of 28.11.2024 as amended by Resolution No. 1638 of 23.10.2025.

Import VAT in EAEU countries

  • Russia22%
  • Kazakhstan16%
  • Belarus20%
  • Armenia20%
  • Kyrgyzstan12%

Standard rate; each country has reduced rates and exemptions for some goods. The duty for the code above is the union one, the same for all

Customs declaration fee

  • Kazakhstan6 MCI per goods declaration, KZT 25,950 in 2026
  • BelarusBYN 120 for goods of chapter 38from Jan 1, 2027: BYN 135
  • ArmeniaAMD 3,500 for clearanceinspection and recording: AMD 1,000 per consignment up to 1 t and AMD 300 per each additional tonne
  • Kyrgyzstan0.4% of the customs valuenot less than 5 and not more than 2,500 calculation units

May be VAT-exempt

The exemption under list No. 1042 applies if the goods match a description on the list; a medical device must also be registered:

  • 3822 19 000 — Тесты для определения COVID-19
Calculate the whole deal →Quick payment calculation →

Tariff preferences

The code is on the EAEU list of preferential goods: for goods originating in a beneficiary country the duty is lower

Least developed countrieszero rate0%
46 countries

Burkina Faso, Guinea, Eritrea, Congo - Kinshasa, Timor-Leste, Afghanistan, Mauritania, Yemen, Cambodia, Lesotho, Laos, Bangladesh, Nepal, Tanzania, Palestinian Territories, Angola, Benin, Burundi, Haiti, Gambia, Guinea-Bissau, Djibouti, Zambia, Kiribati, Liberia, Madagascar, Malawi, Mali, Mozambique, Niger, Rwanda, Senegal, Myanmar (Burma), Sudan, Sierra Leone, Uganda, Chad, South Sudan, Syria, Solomon Islands, Comoros, Togo, Tuvalu, Ethiopia, Somalia, Central African Republic

The preference requires a document of origin and compliance with the direct consignment rule; customs checks the right to it at declaration.

Documents required

A summary across all the lists we check: the document, its legal basis and whether it covers the whole code. Details are in the sections below.

Goods in customs transit may be tracked with a navigation seal: this depends on the route and procedure, not on the code (EAEU Agreement of 19.04.2022, EEC Board Decision No. 84).

Customs declaration hints

Boxes 33, 36, 44, 47

Which codes go into the boxes of the goods declaration for this product. The codes come from the classifiers of Customs Union Commission Decision No. 378. Reliefs, document types and excise depend on the shipment, so such lines carry a condition.

Box 33 · Commodity code

  • 3822190009
  • Сin the second subdivision, if the goods do not fall under the bans and restrictions that apply to the code
  • Оin the second subdivision, if goods with different names are declared under one code

Box 36 · Preference

  • ОООО-ООFees, duty, excise, VAT: no relief claimed, no excise (dash)
  • ООНН-ООТарифная преференция в отношении товаров, происходящих из наименее развитых стран · if the goods originate in a least developed country and origin is proven
  • ОООО-ХТОсвобождение от уплаты НДС в отношении ввозимых в Российскую Федерацию медицинских изделий · if the goods match a description on the VAT exemption list (Resolution No. 1042)

Box 44 · Documents produced

  • 01408Документ об оценке соответствия, предусмотренный законодательством государства – члена Евразийского экономического союза, на территории которого продукция (товар) помещается под таможенные процедуры · Постановление № 2425
  • 06013Сертификат о происхождении товара формы "А" · if the goods are imported under a tariff preference

Box 47 · Calculation of payments

  • 1010Таможенные сборы за совершение таможенных операций (за таможенное оформление товаров, за таможенное декларирование товаров, за таможенные операции)
  • 2010Ввозная таможенная пошлина (иные пошлины, налоги и сборы, имеющие эквивалентное действие), обязанность по уплате которой возникла с 1 сентября 2010 г.
  • 5010Налог на добавленную стоимость

Completion rules and classifiers: Решение Комиссии Таможенного союза от 20.05.2010 № 257; классификаторы — Решение Комиссии Таможенного союза от 20.09.2010 № 378

Each requirement in detailParallel import · Medical devices · Veterinary, plant quarantine and sanitary control · Conformity assessment · How it is certified

Parallel import

The code falls under the list of Order No. 2701 of the Russian Ministry of Industry and Trade: goods put on the market abroad by the right holder or with its consent may be imported without the right holder's consent, but only under the trademarks of the item.

  • Item 49 · 38

    ACURA, ALFA ROMEO, AUDI, BENTLEY, BMW, CADILLAC, CASTROL, CHEVROLET, CHRYSLER, DAEWOO, DAIHATSU, DATSUN, DODGE, elf, FERRARI, FIAT, GENERAL MOTORS (GM), GMC, HONDA, HUMMER, INFINITI, JAGUAR, JEEP, LAND ROVER, LEXUS, LINCOLN, MASERATI, MAYBACH, MERCEDES-BENZ, MINI, MITSUBISHI, NISSAN, PORSCHE, ROVER, SAAB, SEAT, SIEMENS, ŠKODA, SMART, SUBARU, SUZUKI, TESLA, TOTAL, TotalEnergies, TOYOTA, VOLKSWAGEN, VOLVO (except AIR WICK, Finish, Vanish)

  • Item 59 · 3822

    BENTONORIT, FLOP AM, HYDRAIZER (Polymer systems), MAGNAFLOC

Medical devices

If the product is a medical device, it may be imported and sold in Russia only after state registration: with Roszdravnadzor (Article 38 of Federal Law No. 323-FZ) or under EAEU rules (EEC Council Decision No. 46 of 12.02.2016). Whether it is a medical device depends on its intended use, not on the code.

Veterinary, plant quarantine and sanitary control

Goods fall under supervision by their type and characteristics

  • Sanitary and epidemiological supervision (control)

    rule for the whole chapter 38
    Материалы, оборудование, вещества, устройства, применяемые в сфере хозяйственно-питьевого водоснабжения и при очистке сточных вод, в плавательных бассейнах; Химическая и нефтехимическая продукция производственного назначения, продукция (товары) бытовой химии, лакокрасочные материалы; Продукция машиностроения и приборостроения производственного, медицинского и бытового назначения, кроме запасных частей к транспортным средствам и бытовой технике (за исключением контактирующих с питьевой водой и пищевыми продуктами); Пестициды и агрохимикаты; Оборудование, материалы для воздухоподготовки, воздухоочистки и фильтрации; Антигололедные реагенты; Иная продукция (товары), в отношении которой одним из государств – членов Евразийского экономического союза введены временные санитарные меры

    Решение Коллегии Евразийской экономической комиссии от 17.09.2019 № 154

Conformity assessment

May apply

Whether the goods fall under a regulation depends on their name and characteristics. Check them against the list

  • Постановление № 2425Единый перечень продукции: сертификация и декларирование в РФ
    • Препараты диагностические ветеринарные — declaration of conformity (part of the heading) · ГОСТ 16445-2012, ГОСТ Р 52682-2006, ГОСТ 14109-2016
    • Тест-системы для диагностики других инфекционных заболеваний (применяемые в ветеринарии) — declaration of conformity (part of the heading) · ГОСТ Р 51088-2013, ГОСТ 27145-86 (СТ СЭВ 5156-85), ГОСТ Р 51352-2013, ГОСТ Р 58569-2019, ГОСТ Р 70150-2022

Checked: the consolidated list of Government Decree No. 2425 and the lists of 42 technical regulations out of 52 adopted. The others have no list by HS code, so see the full list of regulations.

How it is certified

Valid documents in the EAEU unified register for subheading 3822 19: certificates 0, declarations 8.

By technical regulation
ТР ТС 009/20117ТР ТС 017/20111
Schemes
3д71д1The letter after the scheme number shows the form: certification or declaration of conformity.
Manufacturers outside the EAEU
United States5China4United Kingdom1Japan1

Manufacturers of these goods →Check a supplier’s document by its number →

Export from Russia

Documents required

A summary across all the lists we check: the document, its legal basis and whether it covers the whole code. Details are in the sections below.

Customs declaration hints

Boxes 33, 44, 47

Which codes go into the boxes of the goods declaration for this product. The codes come from the classifiers of Customs Union Commission Decision No. 378. Reliefs, document types and excise depend on the shipment, so such lines carry a condition.

Box 33 · Commodity code

  • 3822190009
  • Оin the second subdivision, if goods with different names are declared under one code

Box 44 · Documents produced

  • 01011Лицензия на экспорт и (или) импорт товаров · Постановление Правительства РФ от 09.03.2022 № 312

Box 47 · Calculation of payments

  • 1010Таможенные сборы за совершение таможенных операций (за таможенное оформление товаров, за таможенное декларирование товаров, за таможенные операции)

Completion rules and classifiers: Решение Комиссии Таможенного союза от 20.05.2010 № 257; классификаторы — Решение Комиссии Таможенного союза от 20.09.2010 № 378

Russian bans and restrictions

May apply

Whether a measure applies to your goods is determined by the provisos in the “code” column. Measures are taken from the register as of the date the act was published; the act is named on every line

  • 3822 (за исключением 3822 90 000 0)Out of RussiaProhibited

    Отдельные виды товаров — временный запрет на вывоз

    Реагенты диагностические или лабораторные на подложке, готовые диагностические или лабораторные реагенты на подложке или без нее, не расфасованные или расфасованные в наборы, кроме товаров товарной позиции 3006; сертифицированные эталонные материалы

    Постановление Правительства РФ от 09.03.2022 № 311 — until Dec 31, 2027

  • 3822 (за исключением 3822 90 000 0)Out of RussiaPermit required

    Товары медицинского назначения

    Реагенты диагностические или лабораторные на подложке, готовые диагностические или лабораторные реагенты на подложке или без нее, не расфасованные или расфасованные в наборы, кроме товаров товарной позиции 3006; сертифицированные эталонные материалы

    Постановление Правительства РФ от 09.03.2022 № 312 — until Dec 31, 2027

Classification

Where it sits in the nomenclature

Section VI. Products of the chemical or allied industries

  1. 38Miscellaneous chemical products
  2. 3822Diagnostic or laboratory reagents on a backing, prepared diagnostic or laboratory reagents whether or not on a backing, and certified reference materials (excl. compound diagnostic reagents designed to be administered to the patient, blood-grouping reagents, animal blood prepared for therapeutic, prophylactic or diagnostic uses and vaccines, toxins, cultures of micro-organisms and similar products)
  3. 3822 19 000 9you are here

Compare the description of your goods with the neighbouring codes on the subheading line above.

Explanatory notes to heading 3822 4 paragraphs

Machine translation from Russian. The original is the EEC explanatory note, and that is what a classification dispute is argued from; the translation is for understanding and has no legal force.

3822 Diagnostic or laboratory reagents on a substrate, prepared diagnostic or laboratory reagents on or without a substrate, other than goods of heading 3002 or 3006; certified reference materials

This heading includes diagnostic or laboratory reagents on a substrate, ready-made diagnostic or laboratory reagents other than diagnostic reagents of heading 3002, diagnostic reagents intended for administration to patients, and blood type reagents of heading 3006. Diagnostic reagents are used for the assessment of physical, biological or biochemical processes and conditions of the human or animal organism; their operation is based on the measurement or observation of changes occurring in the biological or chemical substances contained in the reagent. The finished diagnostic reagents of this heading may be similar to those intended to be administered to patients (subheading 3006 30), except that they are used for in vitro rather than in vivo use. Prepared laboratory reagents

include not only diagnostic reagents but also other analytical reagents used for purposes other than the detection or diagnosis of something. Prepared diagnostic or laboratory reagents may be used in medical, veterinary, scientific or industrial laboratories, in hospitals, in industry, in field laboratories or, in some cases, in the home. The reagents of this heading on a backing or in the form of preparations contain more than one component. For example, they may consist of a mixture of two or more reagents dissolved in solvents other than water. They may also be in the form of paper, plastics or other materials (used as a backing or support) impregnated or coated with one or more diagnostic or laboratory reagents, e.g., litmus paper, pH or polarity indicator paper, plates pre-coated with reagents for immunoassay. The reagents of this heading may be put up in the form of kits consisting of several components, even if one or more of the components are separate chemically defined compounds of Chapter 28 or 29, synthetic colouring matter of heading 3204 or any other substance which, if presented separately, would fall in its appropriate heading. Examples of such kits are those for determining glucose in the blood, ketones in the urine, etc., as well as enzyme-based kits. However, diagnostic kits having the character of goods of heading 3002 or 3006 (e.g., those based on monoclonal or polyclonal antibodies) are excluded from this heading. The reagents of this heading must be clearly identifiable as being for use only as diagnostic or laboratory reagents. Their composition, labelling, instructions for in vitro or laboratory use, the comparison scale for the test or samples (e.g., presented on a backing or support) must be indicated. Except for the goods of Chapter 28 or 29, for the classification of certified reference materials heading 382 2 takes precedence over any other heading of the Nomenclature. The certified reference materials of this heading are reference materials prepared for the calibration of an apparatus, the assessment of a measurement method or the determination of unknown values. These reference materials may consist of: (a) matrix materials to which analytes have been added in precisely determined concentrations; (b) unmixed materials some components of which have a precisely determined concentration (e.g., the protein and fat content in milk powder); (c) natural or synthetic materials some properties of which have been precisely determined (e.g., tensile strength, specific gravity). These reference materials must be accompanied by a certificate, authenticated by the authorities, stating the values of the properties of the certified materials, the methods used to determine these values and the measurement uncertainty of each value. The heading also excludes the following reagents, whether or not put up in forms for use as diagnostic or laboratory reagents: (a) goods of headings 2843 - 2846 and 2852 (see Note 1 to Section VI); (b) goods referred to in Note 1 to Chapter 28 or in Note 1 to Chapter 29; (c) colouring matter of heading 3204, including the products referred to in Note 3 to Chapter 32;

(d) media cultured ready to grow or sustain microorganisms (including viruses and the like) or plant, human or animal cells (heading 3821).

Official text adopted by a Recommendation of the EEC Board

Notes to chapter 38 — Miscellaneous chemical products 11 items

Notes

English text as published in Annex I to Regulation (EU) 2021/1832 (Combined Nomenclature). The EAEU tariff and the EU nomenclature copy these notes from the same convention. For a Russian declaration the binding version is the Russian one: Annex to Decision No 80 of the EEC Council of 14 September 2021.

1. This chapter does not cover:

(a) separate chemically defined elements or compounds with the exception of the following:

(1) artificial graphite (heading 3801);

(2) insecticides, rodenticides, fungicides, herbicides, anti-sprouting products and plant-growth regulators, disinfectants and similar products, put up as described in heading 3808;

(3) products put up as charges for fire-extinguishers or put up in fire-extinguishing grenades (heading 3813);

(4) certified reference materials specified in note 2 below;

(5) products specified in note 3(a) or 3(c) below;

(b) mixtures of chemicals with foodstuffs or other substances with nutritive value, of a kind used in the preparation of human foodstuffs (generally, heading 2106);

(c) products of heading 2404;

(d) slag, ash and residues (including sludges, other than sewage sludge), containing metals, arsenic or their mixtures and meeting the requirements of note 3(a) or 3(b) to Chapter 26 (heading 2620);

(e) medicaments (heading 3003 or 3004); or

(f) spent catalysts of a kind used for the extraction of base metals or for the manufacture of chemical compounds of base metals (heading 2620), spent catalysts of a kind used principally for the recovery of precious metal (heading 7112) or catalysts consisting of metals or metal alloys in the form of, for example, finely divided powder or woven gauze (Section XIV or XV).

2. (A) For the purpose of heading 3822, the expression ‘certified reference materials’ means reference materials which are accompanied by a certificate which indicates the values of the certified properties, the methods used to determine these values and the degree of certainty associated with each value and which are suitable for analytical, calibrating or referencing purposes.

(B) With the exception of the products of Chapter 28 or 29, for the classification of certified reference materials, heading 3822 shall take precedence over any other heading in the nomenclature.

3. Heading 3824 includes the following goods which are not to be classified in any other heading of the nomenclature:

(a) cultured crystals (other than optical elements) weighing not less than 2,5 g each, of magnesium oxide or of the halides of the alkali or alkaline-earth metals;

(b) fusel oil; Dippel's oil;

(c) ink removers put up in packings for retail sale;

(d) stencil correctors, other correcting fluids and correction tapes (other than those of heading 9612), put up in packings for retail sale; and

(e) ceramic firing testers, fusible (for example, Seger cones).

4. Throughout the nomenclature, ‘municipal waste’ means waste of a kind collected from households, hotels, restaurants, hospitals, shops, offices, etc., road and pavement sweepings, as well as construction and demolition waste. Municipal waste generally contains a large variety of materials such as plastics, rubber, wood, paper, textiles, glass, metals, food materials, broken furniture and other damaged or discarded articles. The term ‘municipal waste’, however, does not cover:

(a) individual materials or articles segregated from the waste, for example wastes of plastics, rubber, wood, paper, textiles, glass or metals, electrical and electronic waste and scrap (including spent batteries) which fall in their appropriate headings of the nomenclature;

(b) industrial waste;

(c) waste pharmaceuticals, as defined in note 4(k) to Chapter 30; or

(d) clinical waste, as defined in note 6(a) below.

5. For the purposes of heading 3825, ‘sewage sludge’ means sludge arising from urban effluent treatment plant and includes pre-treatment waste, scourings and unstabilised sludge. Stabilised sludge when suitable for use as fertiliser is excluded (Chapter 31).

6. For the purposes of heading 3825, the expression ‘other wastes’ applies to:

(a) clinical waste, that is, contaminated waste arising from medical research, diagnosis, treatment or other medical, surgical, dental or veterinary procedures, which often contain pathogens and pharmaceutical substances and require special disposal procedures (for example, soiled dressings, used gloves and used syringes);

(b) waste organic solvents;

(c) wastes of metal pickling liquors, hydraulic fluids, brake fluids and anti-freezing fluids; and

(d) other wastes from chemical or allied industries. The expression ‘other wastes’ does not, however, cover wastes which contain mainly petroleum oils or oils obtained from bituminous minerals (heading 2710).

7. For the purposes of heading 3826, the term ‘biodiesel’ means mono-alkyl esters of fatty acids of a kind used as a fuel, derived from animal, vegetable or microbial fats and oils whether or not used.

Subheading notes

English text as published in Annex I to Regulation (EU) 2021/1832 (Combined Nomenclature). The EAEU tariff and the EU nomenclature copy these notes from the same convention. For a Russian declaration the binding version is the Russian one: Annex to Decision No 80 of the EEC Council of 14 September 2021.

1. Subheadings 3808 52 and 3808 59 cover only goods of heading 3808, containing one or more of the following substances : alachlor (ISO); aldicarb (ISO); aldrin (ISO); azinphos-methyl (ISO); binapacryl (ISO); camphechlor (ISO) (toxaphene); captafol (ISO); carbofuran (ISO); chlordane (ISO); chlordimeform (ISO); chlorobenzilate (ISO); DDT (ISO) (clofenotane (INN), 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane); dieldrin (ISO, INN); 4,6-dinitro-o-cresol (DNOC (ISO)) or its salts; dinoseb (ISO), its salts or its esters; endosulfan (ISO); ethylene dibromide (ISO) (1,2-dibromoethane); ethylene dichloride (ISO) (1,2-dichloroethane); fluoroacetamide (ISO); heptachlor (ISO); hexachlorobenzene (ISO); 1,2,3,4,5,6-hexachlorocyclohexane (HCH (ISO)), including lindane (ISO, INN); mercury compounds; methamidophos (ISO); monocrotophos (ISO); oxirane (ethylene oxide); parathion (ISO); parathion-methyl (ISO) (methyl-parathion); pentachlorophenol (ISO), its salts or its esters; perfluorooctane sulphonic acid and its salts; perfluorooctane sulphonamides; perfluorooctane sulphonyl fluoride; phosphamidon (ISO); 2,4,5-T (ISO) (2,4,5-trichlorophenoxyacetic acid), its salts or its esters; tributyltin compounds; trichlorfon (ISO).

2. Subheadings 3808 61 to 3808 69 cover only goods of heading 3808, containing alpha-cypermethrin (ISO), bendiocarb (ISO), bifenthrin (ISO), chlorfenapyr (ISO), cyfluthrin (ISO), deltamethrin (INN, ISO), etofenprox (INN), fenitrothion (ISO), lambda-cyhalothrin (ISO), malathion (ISO), pirimiphos-methyl (ISO) or propoxur (ISO).

3. Subheadings 3824 81 to 3824 89 cover only mixtures and preparations containing one or more of the following substances : oxirane (ethylene oxide); polybrominated biphenyls (PBBs); polychlorinated biphenyls (PCBs); polychlorinated terphenyls (PCTs); tris(2,3-dibromopropyl) phosphate; aldrin (ISO); camphechlor (ISO) (toxaphene); chlordane (ISO); chlordecone (ISO); DDT (ISO) (clofenotane (INN); 1,1,1-trichloro-2,2-bis(p-chlorophenyl)ethane); dieldrin (ISO, INN); endosulfan (ISO); endrin (ISO); heptachlor (ISO); mirex (ISO); 1,2,3,4,5,6-hexachlorocyclohexane (HCH (ISO)), including lindane (ISO, INN); pentachlorobenzene (ISO); hexachlorobenzene (ISO); perfluorooctane sulphonic acid, its salts; perfluorooctane sulphonamides; perfluorooctane sulphonyl fluoride; tetra-, penta-, hexa-, hepta- or octabromodiphenyl ethers; short-chain chlorinated paraffins. Short-chain chlorinated paraffins are mixtures of compounds, with a chlorination degree of more than 48 % by weight, with the following molecular formula : CxH(2x-y+2)Cly, where x=10 – 13 and y= 1 – 13.

4. For the purposes of subheadings 3825 41 and 3825 49, ‘waste organic solvents’ are wastes containing mainly organic solvents, not fit for further use as presented as primary products, whether or not intended for recovery of the solvents.

Classification rulings for this code (13)

Machine translation from Russian. The original is the Russian wording of the ruling, and customs goes by it; this translation is for understanding only and has no legal force.

The set of calibrators is designed to calibrate a set of reagents for the determination of low-density lipoprotein (LDL) cholesterol during in vitro diagnostics performed on biochemical analyzers.

Full description

The set of calibrators contains 3 bottles of 2 ml of calibrator (lyophilized albumin-based product from bovine serum in the buffer ~ 99.9985%, human cholesterol from low-density lipoproteins ~ 0.0015%). A set of calibrators with a list of values of the parameters of the calibrator series is packed in a cardboard box, marked.

GRI 1 and 6

Одноразовая кассета для Модулей синтеза F применяется в позитронно-эмиссионной томографии (ПЭТ) для получения в результате синтеза кассеты в Модулях синтеза раствора «[18Ф]фтормизонизадола», применяемого для ПЭТ диагностики в определении степени гипоксии злокачественных опухолей, в том числе для планирования и контроля лучевой терапии.

Full description

Кассета содержит 25-клапанный запорный коллектор, два шприца по 6 мл, один шприц 1 мл, соединения для входящих и исходящих жидкостей, разъемы для соединения с флаконами с реагентами (смесь элюента, содержащая гидрокарбонат тетрабутиламмония (0,8 мл), ацетонитрил (4,2 мл), фосфорная кислота (4,2 мл), этанол (4,0 мл)) и три картриджа для твердофазной экстракции со светло-голубым кольцом, с серым кольцом, с зеленым кольцом).

В комплект поставки входит лист с сертификатом анализа, защитная упаковка с собственно кассетой, входной фильтр для азота, а также дополнительные одноразовые элементы: входной фильтр для азота (белый), прекурсор NITTP (формула: 3-(2-нитроимидазол-1-ил)-2-О-тетрагидропиранил-1-О-толуолсульфохлоридпропанедиол; флакон 7,0 мг, вставляется в слот кассеты и присоединяется через разъем с помощью иглы и трубки, находящейся на корпусе кассеты), флакон воды для инъекций (100 мл). Кассета упакована по 5 штук в коробку, помещенную совместно с коробкой с 5 флаконами прекурсора NITTP в транспортную коробку.

GRI 1 and 6

The set of calibrators is designed for in vitro diagnostics for determining neuron-specific enolase (NSE) and is used to calibrate the test on the analyzers of the series "...".

Full description

The calibration set shall contain: 1) Calibrator with a low concentration of 2 vials of 2.0 ml (Neuron-specific enolase antigen (NSE) (human) ~ 0.000034%, bovine serum albumin ~1.0%, sodium phosphate ~ 0.5%, potassium phosphate ~0.18%, Xylitol (preservative) ~1.0%, sodium azide ~0.09%, water ~97.229966%); 2) Calibrator with a high concentration of 2 vials of 2.0 ml (Neuron-specific enolase antigen (NSE) ~ 0.0027%, bovine serum albumin ~1.0%, sodium phosphate ~ 0.5%, potassium phosphate ~0.18%, Xylitol (preservative) ~1.0%, sodium azide ~0.09%, water ~97.2273%).

A set of calibrators with a list of values of the calibrator batch parameters is packed in a cardboard box, marked.

GRI 1 and 6

The set of calibrators is designed for in vitro diagnostics when calibrating CHE, GGT, LDLP and Lip assays using biochemical series analyzers.

Full description

The calibration set shall contain: 6 bottles of dark glass with a screwing green cover of 2.5 ml of calibrator (bull serum albumin ~ 6.0%, amphotericin B ~ 0.000231%, lipase (pig pancreas) ~ 0.48%, α-amylase (human pancreas) ~ 3.876%, gamma-glutamyltranspeptidase (bovine kidney) ~ 5.712%, lactate dehydrogenase (LDHL) (chicken heart) ~ 5.04% pseudocholinesterase (CHE) (horse serum) ~ 35.5% water ~ 43.391769%. A set of calibrators with a list of values of the calibrator batch parameters is packed in a cardboard box, marked.

GRI 1 and 6

The in vitro reagent "..." is intended for use as a control in heparin analysis methods (monitoring the effectiveness of heparin therapy, adjusting the dose of heparin, measuring the performance of the ARTT test (activated partial thromboplastin time).

Full description

After recovery (dilution) of 1 ml of distilled or deionized water, each vial contains: human plasma 3%, sodium citrate 2%, heparin 0.06%, sodium chloride 2%, Tris/HCl 3%, preservative 5-chloro-2-methyl-4-isothiazole-3-on 0.0001%, preservative 2-methyl-4-isothiazole-3-on 0.00005%, sodium azide preservative 0.05%, water 89.89%. Release form: 1 ml of the reagent in a vial with a screwing lid of lilac color, 10 vials in a cardboard box, marked.

GRI 1 and 6

The in vitro reagent "..." is intended for use as a control in heparin analysis methods (monitoring the effectiveness of heparin therapy, adjusting the dose of heparin, measuring the performance of the ARTT test (activated partial thromboplastin time).

Full description

After recovery (dilution) of 1 ml of distilled or deionized water, each vial contains: human plasma 3%, sodium citrate 2%, heparin 0.02%, sodium chloride 2%, Tris/HCl 3%, preservative 5-chloro-2-methyl-4-isothiazole-3-on 0.0001%, preservative 2-methyl-4-isothiazole-3-on 0.00005%, sodium azide preservative 0.05%, water 89.93%. Release form: 1 ml of reagent in a vial with a screwing blue lid, 10 vials in a cardboard box, with the marking applied.

GRI 1 and 6

Одноразовая кассета для Модуля синтеза применяется в позитронно-эмиссионной томографии для получения в результате синтеза кассеты в Модуле синтеза раствора «3'-дезокси-3'-[F-18] фтортимидин:», применяемого в качестве радиофармацевтического зонда системы визуализации, для количественной оценки клеточной пролиферации в злокачественных опухолях.

Full description

Кассета содержит 25-клапанный запорный коллектор, два шприца по 6 мл, один шприц 1 мл, соединения для подачи и вывода жидкостей, шипы портов для подключения к флаконам с реагентами (элюент (0,8 мл), ацетонитрил (4,2 мл), фосфорная кислота (4,2 мл), этанол (4,0 мл)) и пять твердотелых экстракционных картриджей (QMA (с голубым кольцом), PS-H+ (прозрачный с бежевым порошком, без кольца), (с оранжевым кольцом), (с серым кольцом), Alumina A (с кольцом цвета зеленого яблока)).

В комплект поставки входит лист с Сертификатом анализа, защитная упаковка с собственно кассетой, входной фильтр для азота, а также дополнительные одноразовые элементы: входной фильтр для азота (белый), прекурсор 3-N-Boc-5ʼ-О-диметокситритил-3ʼ-О-нозил-тимидин (флакон 20±0,5 мг, вставляется в слот кассеты и присоединяется через разъем с помощью иглы и трубки, находящейся на корпусе кассеты), пакет воды для инъекций (100 мл). Кассета упакована по 5 штук в коробку, помещенную совместно с коробкой с 5 флаконами прекурсора (3-N-Boc-5ʼ-О-диметокситритил-3ʼ-О-нозил-тимидин) в транспортную коробку.

GRI 1 and 6

Disposable cassette ... for Synthesis Module ..., designed for the synthesis of two separate series of solution [18F]2-fluoro-2-deoxy-D-glucose ([18F]FDG), used as a diagnostic tool in positron emission tomography (PET) to determine impaired glucose metabolism, which allows to assess malignancy in patients who, according to the results of other research methods, have certain disorders, as well as in patients with an established cancer diagnosis.

Full description

The cassette consists of: the cassette body; reaction tanks; cartridges for cleaning the solid phase: anion-exchange cartridge - QMA light (2 pcs), environmental cartridge ..., cartridge ..., aluminum-oxide cartridge ... (2 units); molded cassette lining; six bottles of reagents, containing, respectively: eluent (1.4 ml), ethanol (2.5 ml), mannose triflate (4.0 ml), sodium hydroxide (4.0 ml), acetonitrile (4.0 ml), Limon acid buffer (4.3 ml); silicone tube with connecting elements (length 14 cm, 5 pcs), silicone tube with connecting elements (length 11 cm, 2 pcs), silicone tube with connecting elements (length 42 cm, 3 pcs), silicone tube with connecting elements (length 30 cm) and soft container for water with a spike.

Included with the cassette are: nitrogen filter (in individual packaging) and water bottle for injection (250 ml). Cassette ... packed with 5 pieces in a cardboard box.

GRI 1 and 6

Disposable cassette ... for Synthesis Module ... and ... used in positron emission tomography (PET) to obtain as a result of the synthesis of the cassette in the Synthesis Module ... and ... radiochemical solution [18F] FDG fluorodeoxyglucose used as a diagnostic tool for the study and diagnosis of cancer (staging, monitoring during treatment (response to therapy), observation after treatment), diagnosis of cardiovascular diseases (determination of myocardial viability) and neurological diseases (dement).

Full description

The cassette contains a 25-valve shut-off manifold, two syringes of 6 ml, one syringe 1 ml, connections for supply and withdrawal of liquids, port spikes for connection to five bottles with reagents (eluent mixture, containing Kryptofix®, potassium carbonate, acetonitrile and water (850 μl); mannose triflate (2.0 ml); ethanol (4.0 ml); sodium hydroxide (4.2 ml); citrate buffer solution (4.3 ml) and four solid-state extraction cartridges (QMA (light blue ring) for incoming activity; ambient tC18 (with a red ring) tC18 plus (with a red ring)

Alumina N (with a light green ring)

The package includes: a certificate, a hard plastic sheet containing the cassette itself, an air filter in a double sealed plastic bag, a bottle with 100 ml of sterile water for injection. The tape is packed in 10 pieces in a transport box.

GRI 1 and 6

Disposable cassette ... for Synthesis Module ... intended for the synthesis of [18F]sodium fluoride ([18F]NaF), used as a diagnostic tool in positron emission tomography (PET) to assess malignancy in patients who, according to the results of other research methods, have been identified or suspected certain disorders, as well as in patients with an established cancer diagnosis.

Full description

The cassette consists of a 25-valve switchgear collector, two syringes with a volume of 6 ml, one syringe with a volume of 1 ml, connectors for the introduction and removal of liquid, needles for connection with ampoules containing reagents, a cartridge with a solid phase. Included with the cassette are: insert with a certificate of analysis, holder with a cassette, and additional disposable components (filter for incoming nitrogen (white), ampoule for collection of the product and the output filter (white), 0.22 μm output filter (blue), ampoule with sterile water (4 ml), a package with 0.9% sodium chloride (volume of at least 100 ml), ampoule for collection, two needles.

The cassette ... is packed in a plastic casing and in an individual package of coated cardboard of 10 pieces in a transport cardboard box.

GRI 1 and 6

Disposable cassette ... for the Synthesis Module ... and ... used in positron emission tomography to obtain as a result of the synthesis of the cassette in the Synthesis Module ... and ... radiochemical solution [18F] FDG fluorodeoxyglucose, used as a diagnostic tool for the study and diagnosis of cancer (staging, monitoring during treatment (response to therapy), observation after treatment), diagnosis of cardiovascular diseases (determination of myocardial viability) and neurological diseases (dementia).

Full description

The cassette contains a 25-valve shut-off manifold, reaction vessel, two syringes of 6 ml each, one 1 ml syringe, connections for incoming and outgoing liquids, connectors for connection with five bottles with reagents (mixture of eluent, containing ... potassium carbonate, acetonitrile and water (850 μl); mannose triflate in MecN (2.0 ml); acetonitrile (4.2 ml); sodium hydroxide (4.2 ml); phosphoric acid (4.3 ml) connector for connection to the water bag and four cartridges (QMA (light blue ring) for incoming activity, cartridge tC18 (red ring), cartridge ...

HLB (red ring), cartridge (light green ring)

The package includes: a certificate, a hard plastic sheet containing the cassette itself, an air filter in a double sealed plastic bag, a bottle with 100 ml of sterile water for injection. The tape is packed in 10 pieces in a transport box.

GRI 1 and 6

A test sample for urine biochemistry is a reagent for in vitro diagnostics in the form of yellow powder obtained from vacuum-dried (lyophilized) human urine of a large number of anonymized people with the addition of a number of substances (potassium, calcium, albumin, glucose, citrate...).

Full description

It does not contain blood and blood components in the composition, as well as immunological components. The product is intended for biochemical research in clinical diagnostic laboratories.

It is supplied in glass bottles with a screw cover of 5 ml. The bottle is packed in a laminated box with identification labels, which also includes user instructions, as well as insert sheets with the values of analytical parameters, permissible boundaries, deviations and traceability of reference materials (with indication of methods, units of measurement and permissible spreads).

GRI 1 and 6

A test sample for urine biochemistry is a reagent for in vitro diagnostics in the form of yellow powder obtained from vacuum-dried (lyophilized) human urine of a large number of anonymized people with the addition of a number of substances (potassium, calcium, albumin, glucose, citrate...).

Full description

It does not contain blood and blood components in the composition, as well as immunological components. The product is intended for biochemical research in clinical diagnostic laboratories.

It is supplied in glass bottles with a screw cover of 5 ml. The bottle is packed in a laminated box with identification labels, which also includes user instructions, as well as insert sheets with the values of analytical parameters, permissible boundaries, deviations and traceability of reference materials (with indication of methods, units of measurement and permissible spreads).

GRI 1 and 6

Rulings of other EAEU countries for this code (13)

An advance ruling binds only the country that issued it, but it shows how neighbours in the Union classify this product.

The EEC publishes these rulings in Russian only, and they are shown as published.

Kazakhstan

Maternal Health Control, I trimester представляет собой контрольную лиофилизированную сыворотку крови человека.

Full description

Производится из крови человека с добавлением составляющими человеческого происхождения. Кровь берется в контролируемых условиях в гематологических центрах. Продукт содержит менее 1 ммоль/л хлоридов бензамидиниума. Используется в качетсве контрольного материала in vitro для обеспечения точности и правильности лабораторных измерений свободной ß- субъединицы хорионического гонадотропина человека (ß-hCG, free) и ассоциированного с беременностью протеина-А плазмы (PAPP-A) в рамках скрининга беременных в I триместре. Применяется в методиках количественного, полуавтоматического и автоматического иммунологическог…

ОПИ 1 и 6

Kazakhstan

Вторичный стандартный образец этелкальцетид гидрохлорид (марка Аmgen, модель AMG 416, арт. 4107394, модификация Secondary Reference Standard) ) представляет собой надлежащим образом охарактеризованный стандартный образец установленного качества и чистоты, аттестованный путём сравнения (калибровки) с первичным стандартным образцом.

Full description

Применяется для лабораторных испытаний in vitro при проведении рутинных анализов контроля качества лекарственного препарата Парсабив. Этелкальцетид гидрохлорид (AMG 416 гидрохлорид) - пептид, являющийся активатором кальций-чувствительного рецептора (CaSR).

Состав раствора этелкальцетида (AMG 416) гидрохлорид (концентрация чистого пептида 1,0 мг/мл) растворенный в 10 мМ янтарной кислоте, pH доведено до 4,0 с помощью 1N NaOH или 1N HCl. Прозрачная бесцветная жидкость, упакованная в пластиковый флакон с пластиковой винтовой крышкой (2 мл.). Не содержит веществ животного или человеческого происхождения. Не является лекарственным средством. Производитель — Bachem AG., Швейцария.

ОПИ 1 и 6

Kazakhstan

Дарбэпоэтин альфа (марка Аmgen AMG 033, модель дарбэпоэтин альфа, арт.Lot №0010586289, модификация Primary Reference Standard) представляет собой рекомбинантный человеческий белок – агонист рецептора эритропоэтина, полученный при помощи технологии клеток яичника китайского хомяка.

Full description

Прозрачный бесцветный раствор упакован в стеклянный флакон 2R (0,4 гр.), укупоренный резиновой пробкой с тефлоновым покрытием, обжатой алюминиевым колпачком с отрывной пластиковой крышкой. Стандартный образец дарбэпоэтин альфа (AMG 033) предназначен для лабораторных испытаний in vitro и используется при количественном определении содержания белка методом ИФА при анализе препарата Аранесп.

Состав: концентрация рекомбинантного белка 2 мг/мл., вспомогательные вещества: натрия фосфат 20мМ, натрия хлорид 140мМ, вода для инъекции, рН раствор 6,0.

Состав в процентном отношении дарбэпоэтин альфа (основное вещество) - 98%, сродственные примеси (варианты белка, деградационные продукты) - 2%. Не является лекарственным средством. Производитель — Amgen Inc., США.

ОПИ 1 и 6

EEC decisions on this code

Rates, trade defence measures, licensing and classification: decisions since 2016 whose text names code 3822190009.

Titles of acts are given in Russian as published: this is how they are cited in customs documents.

  • Duties and rates

    Решение Совета ЕЭК № 13

    О внесении изменений в единую Товарную номенклатуру внешнеэкономической деятельности Евразийского экономического союза и Единый таможенный тариф Евразийского экономического союза, а также в решения Комиссии Таможенного союза в отношении отдельных товаров, предназначенных для кожевенно-обувной и химической промышленности, и в некоторые решения Высшего Евразийского экономического совета и Совета Евразийской экономической комиссии

    adopted Jan 30, 2026 · published Feb 26, 2026 · entered into force Mar 8, 2026

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