EU Combined Nomenclature · CN code · HS 3002.12

3002 12 00

3002 12 00: Antisera and other blood fractions

Antisera and blood fractions

✓ Can be used in a customs declaration Data: EU Combined Nomenclature, in force from 1 January 2026 · checked on 24 October 2026

  1. 3002 Human blood; animal blood prepared for therapeutic, prophylactic or diagnostic uses; antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes; vaccines, toxins, cultures of micro-organisms (excluding yeasts) and similar products; cell cultures, whether or not modified:
  2. Antisera, other blood fractions and immunological products, whether or not modified or obtained by means of biotechnological processes:
  3. 3002 12 00 Antisera and other blood fractions

What you pay

Importing into EU

Customs duty Free standard rate depends on the country of origin
Additional duties and charges 2 additional measures Import requirements: 5
VAT standard rate of the member state of import, 17% to 27%
Duty calculatorCalculate duty and taxes →

Additional duties and import rules

Charges on top of the customs duty, and rules the goods must meet at the border.

Additional duties and charges 3

  • Duty on low-value parcelsLow-value consignment customs duty 3 EUR
    Applies to goods from
    all countries
    In force
    until 31 October 2026
    Legal act
    Regulation 0382/26
  • Duty on low-value parcelsLow-value consignment customs duty 3 EUR
    Applies to goods from
    all countries
    In force
    from 1 November 2026
    Legal act
    Regulation 0382/26
    Documents
    • C127 Merchant product identifier
    • C128 Non-standardised manufacturer product identifier
    • C129 Standardised manufacturer product identifier
    • Y081 No standardised manufacturer product identifier for the declared product exists
  • Handling feeUnion handling fee 2 EUR
    Applies to goods from
    all countries
    In force
    from 1 November 2026
    Legal act
    Regulation 2108/26
    Documents
    • Y126 Goods sold in distance sales

Import requirements 6

  • Import controlVeterinary control
    Applies to goods from
    all countries except Andorra, Switzerland, Faroe Islands, Greenland, Iceland, Liechtenstein, Norway, San Marino
    Legal act
    Regulation 0632/21
    Documents
    • N853 Common Health Entry Document for Products (CHED-P) (as set out in Part 2, Section B of Annex II to Commission Implementing Regulation (EU) 2019/1715 (OJ L 261))
    • Y058 Exemption by virtue of Article 7 of Commission Delegated Regulation 2019/2122 (Goods which form part of passengers' personal luggage and are intended for personal consumption or use) or Article 10 (small consignments of goods sent to natural persons which are not intended to be placed on the market) of Commission Delegated Regulation 2019/2122
    • Y170 Goods with third country origin coming from Andorra, according to the relevant EU legislation.
    • Y171 Goods with third country origin coming from Switzerland, according to the relevant EU legislation.
    • Y174 Goods with third country origin coming from Iceland, according to the relevant EU legislation.
    • Y175 Goods with third country origin coming from Liechtenstein, according to the relevant EU legislation.
    • Y176 Goods with third country origin coming from Norway, according to the relevant EU legislation.
    • Y177 Goods with third country origin coming from San Marino, according to the relevant EU legislation.
    • Y930 The declared goods are not concerned by Commission Implementing Regulation (EU) 2021/632
    • C084 Exemption by virtue of Articles 3 and 4 of regulation 2019/2122 (animals intended for scientific purposes, research and diagnostic samples, and samples for product analysis and quality testing).
  • Import controlVeterinary control
    Applies to goods from
    Faroe Islands, Greenland
    Legal act
    Regulation 0632/21
    Documents
    • N853 Common Health Entry Document for Products (CHED-P) (as set out in Part 2, Section B of Annex II to Commission Implementing Regulation (EU) 2019/1715 (OJ L 261))
    • Y058 Exemption by virtue of Article 7 of Commission Delegated Regulation 2019/2122 (Goods which form part of passengers' personal luggage and are intended for personal consumption or use) or Article 10 (small consignments of goods sent to natural persons which are not intended to be placed on the market) of Commission Delegated Regulation 2019/2122
    • Y170 Goods with third country origin coming from Andorra, according to the relevant EU legislation.
    • Y171 Goods with third country origin coming from Switzerland, according to the relevant EU legislation.
    • Y174 Goods with third country origin coming from Iceland, according to the relevant EU legislation.
    • Y175 Goods with third country origin coming from Liechtenstein, according to the relevant EU legislation.
    • Y176 Goods with third country origin coming from Norway, according to the relevant EU legislation.
    • Y177 Goods with third country origin coming from San Marino, according to the relevant EU legislation.
    • Y930 The declared goods are not concerned by Commission Implementing Regulation (EU) 2021/632
    • C084 Exemption by virtue of Articles 3 and 4 of regulation 2019/2122 (animals intended for scientific purposes, research and diagnostic samples, and samples for product analysis and quality testing).
  • Import controlImport control - CITES
    Applies to goods from
    all countries
    Legal act
    Regulation 0966/23
    Documents
    • C400 Presentation of the required " CITES" certificate
    • Y900 Declared goods do not belong to the Washington Convention (CITES)
  • Import control
    Applies to goods from
    Ukraine
    Legal act
    Regulation 0692/14
    Documents
    • Y997 Goods not originating from or destined to Crimea or Sevastopol (Articles 2 and 2b.1 of Council Regulation (EU) No 692/2014)
    • N864 Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document
    • N954 Movement certificate EUR.1
  • Import controlImport control on REACH
    Applies to goods from
    all countries
    Legal act
    Regulation 1907/06
    Documents
    • Y106 Compliance with the REACH restrictions defined in Column 2 of Annex XVII of Regulation (EC) No 1907/2006
    • Y110 Exemption from REACH restrictions by virtue of Article 67(1) and 67(2) of Regulation (EC) No 1907/2006
    • Y113 Substance/mixture not subjected to the provisions of Regulation (EC) No 1907/2006 (Annex XVII)
  • Import control
    Applies to goods from
    Ukraine
    Legal act
    Regulation 0263/22
    Documents
    • Y984 Goods not originating from or not destined for the non-government controlled areas of Ukraine in the oblasts of Donetsk, Kherson, Luhansk and Zaporizhzhia
    • N954 Movement certificate EUR.1
    • N864 Invoice declaration or origin declaration made out by any exporter on invoice or any other commercial document

Export measures 2

Prohibitions, licences, controls and sanctions that apply when these goods leave the EU.

Export measuresDestinationLegal actValidity
Export controlSanctions regime: Russia Russia Regulation 0833/14 1 December 2024
Export control - CITES All third countries Regulation 0966/23 20 May 2023

TARIC data as of 26 October 2026

Import VAT in the EU member states

The rate each member state applies to goods of this code, from the Commission’s Taxes in Europe Database. A reduced rate can cover only part of the goods under a code: check the national VAT law.

  • Austria 0% reduced rate
  • Belgium 6% reduced rate
  • Bulgaria 20%
  • Croatia 5% reduced rate
  • Cyprus 5% reduced rate
  • Czechia 12% reduced rate
  • Denmark 25%
  • Estonia 9% reduced rate
  • Finland 25.5%
  • France 2.1% / 10% reduced rate
  • Germany 19%
  • Greece 0% / 6% / 13% reduced rate
  • Hungary 5% reduced rate
  • Ireland 0% reduced rate
  • Italy 22%
  • Latvia 12% reduced rate
  • Lithuania 5% reduced rate
  • Luxembourg 17%
  • Malta 0% / 5% reduced rate
  • Netherlands 9% reduced rate
  • Poland 23%
  • Portugal 23%
  • Romania 11% reduced rate
  • Slovakia 5% reduced rate
  • Slovenia 9.5% reduced rate
  • Spain 21%
  • Sweden 25%

TEDB · 26 October 2026

EU: imports by month · HS 3002.12

last 12 months€7.1bn-23.9% · previous 12 months
Average import price€232.22 per kg
Preferential rate0%
Jan 2024: €775.5mFeb 2024: €776.6mMar 2024: €739.6mApr 2024: €828.6mMay 2024: €842.8mJun 2024: €888.3mJul 2024: €830.8mAug 2024: €656.3mSept 2024: €812.4mOct 2024: €738.3mNov 2024: €692.4mDec 2024: €746.1mJan 2025: €1.2bnFeb 2025: €682.8mMar 2025: €857.8mApr 2025: €889.4mMay 2025: €803.3mJun 2025: €769.7mJul 2025: €678.4mAug 2025: €442mSept 2025: €566.2mOct 2025: €641.5mNov 2025: €552.3mDec 2025: €527.2mJan 2026: €602.1mFeb 2026: €543.4mMar 2026: €697.9mApr 2026: €604.2mMay 2026: €581.8mJun 2026: €680.7mJul 2026: €562.4mAug 2026: €553.1m 202420252026
Data up to August 2026 (provisional) · Monthly data: Eurostat Comext (CC BY 4.0), HMRC (OGL v3.0)

Main suppliers, last 12 months

CountryValueShareChange
United States €6.2bn 87.3% -3.4%
Switzerland €262.7m 3.7% -88.4%
United Kingdom €141.2m 2% -14.6%
Australia €113.1m 1.6% -20.7%
Egypt €95.3m 1.3% +34.3%
Israel €74.2m 1% +20.1%
New Zealand €53.3m 0.7% +23.7%
Iran €50.2m 0.7% +12.6%

Same subheading in other tariffs

3002.12 Antisera and other blood fractions

Binding rulings for similar goods

Decisions of U.S. Customs and Border Protection (CROSS) and HMRC (Advance Tariff Rulings) on goods classified here. A ruling binds only its holder, but shows how the authorities classify similar goods. The descriptions are the authorities’ own, in English.

  • N333558 U.S. CBP 27 June 2023 · 3002.12.00.90

    The tariff classification of ELOCTATE® [Antihemophilic factor (recombinant), Fc fusion protein] in dosage form, from the United States

  • N304133 U.S. CBP 4 November 2019 · 3002.12.00.90

    The tariff classification of Andexanet Alfa in bulk form, from Spain

  • N294982 U.S. CBP 3 August 2018 · 3002.12.00.90

    The tariff classification of IgG Rabbit Gamma Globulin (Millipore Cat #PP63-K). No country of origin was provided.

  • H259355 U.S. CBP 19 December 2017 · 3002.12.00

    Request for a ruling; Classification of reference materials used in VITROS systems

  • 600011309 HMRC 5 November 2024 – 4 November 2027 · 3002 12 00 00

    Peripheral Blood Mononuclear Cells or any blood cell with a single nucleus These samples are used for clinical trails, laboratory research and diagnostic testing Packaged using Cell Preparation Tubes or standard sample collection tubes

  • 600011305 HMRC 27 August 2024 – 26 August 2027 · 3002 12 00 00

    Human blood fractions Samples of plasma and serum Use: clinical trials, laboratory research or diagnostic purposes Packaging: in test tubes or blood collection tubes

7 rulings in total for this code

Legal notes

Notes
Subheading notes

Chapter notes: Chapter 30 →

CN Explanatory Notes

The European Commission's explanatory notes on how to classify goods in these CN codes. They are not legally binding but customs authorities follow them; they complement the HS Explanatory Notes of the World Customs Organization.

3002 12 00 · Antisera and other blood fractions

This subheading covers the products described in the HS Explanatory Note to heading 3002, (C), (1), second and third paragraph.

This subheading includes ‘normal’ sera, plasma, fibrinogen, fibrin and, provided that it is prepared for therapeutic or prophylactic uses, blood albumin (for example, obtained by fractionating the plasma of human blood).

Blood albumin not prepared for therapeutic or prophylactic uses is, therefore, excluded (note 1(h) to this chapter) (heading 3502).

It does not include sera used as reagents to determine blood groups or blood factors (heading 3006).

General notes to the chapter

PHARMACEUTICAL PRODUCTS

General

The description of a product as a medicament in Union legislation (other than that relating specifically to classification in the Combined Nomenclature) or in the national legislation of the Member States, or in any pharmacopoeia, is not the deciding factor in so far as its classification in this chapter is concerned.

Additional note 1

1. Herbal medicinal preparations are preparations based on one or more active substances, produced by subjecting a plant or parts thereof to a process such as drying, crushing, extraction or purification.

Active substance means a chemically defined substance, a chemically defined group of substances (for example, alkaloids, polyphenols, anthocyanins) or a plant extract. These active substances must have medicinal properties for the prevention or the treatment of specific diseases, ailments or their symptoms.

2. Homeopathic medicinal preparations are prepared from products, substances or compositions called homeopathic stocks (mother tinctures). The degree of dilution must be indicated (for example, D6).

3. Vitamins or mineral preparations are preparations based on vitamins of heading 2936, on minerals including trace elements and mixtures thereof. They are used to treat or prevent specific diseases, ailments or their symptoms. Such preparations contain a much higher amount of vitamins or minerals, generally at least three times higher than the recommended daily allowance (RDA).

As regards the recommended daily allowance (RDA) for certain vitamins and minerals, see, for example, the table in the Annex XIII to Regulation (EU) No 1169/2011 of the European Parliament and of the Council of 25 October 2011 on the provision of food information to consumers (OJ L 304, 22.11.2011, p. 58) reproduced below:

Vitamins and mineralsRDA
Vitamin A800 μg
Vitamin D5 μg
Vitamin E12 mg
Vitamin K75 μg
Vitamin C80 mg
Thiamin1,1 mg
Riboflavin1,4 mg
Niacin16 mg
Vitamin B61,4 mg
Folic acid200 μg
Vitamin B122,5 μg
Biotin50 μg
Pantothenic acid6 mg
Potassium2 000 mg
Chloride800 mg
Calcium800 mg
Phosphorus700 mg
Magnesium375 mg
Iron14 mg
Zinc10 mg
Copper1 mg
Manganese2 mg
Fluoride3,5 mg
Selenium55 μg
Chromium40 μg
Molybdenum50 μg
Iodine150 μg

4. Recommended daily allowance (RDA) for adults with a weight of 70 kg, on essential amino acids, according to the joint WHO/FAO/UNU expert Consultation 2007:

Essential Amino AcidRDA (mg)
Histidine700
Isoleucine1 400
Leucine2 730
Lysine2 100
Methionine + Cysteine1 050
Cysteine287
Methionine728
Phenylalanine + Tyrosine1 750
Threonine1 050
Tryptophan280
Valine1 820

Recommended daily allowance (RDA) for adults with a weight of 70 kg, on essential fatty acids, according to the joint WHO/FAO/UNU expert Consultation 2007.

Types of essential fatty acidsName of essential fatty acidRDA (g)
n-3 polyunsaturated fatty acidslinolenic acid (ALA)2
long-chain n-3 polyunsaturated fatty acidsEPA plus DHA0,25
n-6 polyunsaturated fatty acidslinoleic acid10

Heading 3004 does not cover, inter alia, food supplements or dietary preparations (see also note 1(a) to this chapter).

Explanatory Notes to the Combined Nomenclature of the European Union, Official Journal C (consolidated text and later amendments) · © European Union

This line in earlier years

The Combined Nomenclature of each year, as published in the Official Journal: description, third-country duty and supplementary unit.

YearDescriptionThird-country dutySupplementary unit
2026 Antisera and other blood fractions Free —
2025 unchanged Free —
2024 unchanged Free —
2023 unchanged Free —
2022 unchanged Free —
2021 unchanged Free —
2020 unchanged Free —
2019 Antisera and other blood fractions Free —

Code history

Since 2017; before, these goods were classified under 3002 10 10, 3002 10 91, 3002 10 98.

CN code 3002 12 00 is a line of the EU Combined Nomenclature under HS subheading 3002.12 (antisera and other blood fractions).

The third-country duty is free, and quantities are declared in —.

Imports of antisera and blood fractions (HS 3002.12) into the EU came to €7.1bn between September 2025 and August 2026 (down 24% on the year before); United States supplied 87%, followed by Switzerland.

For the same subheading, the UK duty is free, the Türkiye duty is free, the US duty is free, the Canada duty is free, the Mexico duty is 0%–15%, the Brazil duty is 0%–7.2%, the Argentina duty is 0%–7.2%, the Peru duty is free, the New Zealand duty is free, the Japan duty is free, the Taiwan duty is free, the GCC duty is free, the Switzerland duty is free, the Norway duty is free, the North Macedonia duty is free and the Nigeria duty is free.

EU member states imported goods of subheading 3002.12 worth US$22bn in 2024; the largest supplier from outside the EU was the United States, and the United Kingdom ranked 3rd with US$195m.

Questions and answers

What is the EU import duty for CN code 3002 12 00?

The third-country duty in the EU Combined Nomenclature is free; the supplementary unit is —. Preferential rates for goods from agreement countries, anti-dumping duties and VAT are not included.

Where does the EU import these goods from?

For subheading 3002.12 as a whole, the largest supplier from outside the EU in 2024 was the United States (US$7bn), followed by Switzerland.

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Typical products

Everyday names, not part of the legal text.