Turkish Customs Tariff Schedule · GTİP code · HS 3002.90
3002.90.30.00.00: Other blood products, toxins etc.: Tedavide, korunmada veya teşhiste kullanılmak üzere hazırlanmış hayvan kanı
Other blood products, toxins etc.
✓ Can be used in a customs declaration Data: Turkish Customs Tariff Schedule, in force from 1 January 2026 · checked on 24 October 2026
This line has no official text in this language; it is shown in the language of its tariff.
- 3002 İnsan kanı; tedavide, korunmada veya teşhiste kullanılmak üzere hazırlanmış hayvan kanı; antiserum ve diğer kan fraksiyonları ve bağışıklık sağlayan ürünler (biyoteknolojik işlemle el- de edilmiş olsun olmasın) aşılar, toksinler, mikroorganizma kültürleri (mayalar hariç) ve benzeri ürünler; hücre kültürleri (değiştitirilmiş olsun olmasın):
- 3002.90 Diğerleri:
- 3002.90.30.00.00 Tedavide, korunmada veya teşhiste kullanılmak üzere hazırlanmış hayvan kanı
What you pay
Importing into Türkiye
Rates for Türkiye are the applied duties of the 2026 Import Regime Decision, as consolidated by the Ministry of Trade (amendments to August 2026). The additional customs duty (İGV) and, for some farm goods, the additional financial liability (EMY) come on top. Footnotes can lower a rate for named countries or periods: see the line page.
Additional duties and import rules
Charges on top of the customs duty, and rules the goods must meet at the border.
Import requirements 2
- Import controlİnsan kanı; tedavide, korunmada veya teşhiste kullanılmak üzere hazırlanmış hayvan kanı; antiserum ve diğer kan fraksiyonları ve bağışıklık sağlayan ürünler (biyoteknolojik işlemle elde edilmiş olsun olmasın) aşılar, toksinler, mikroorganizma kültürleri (mayalar hariç) ve benzeri ürünler (veteriner biyolojik ürünler hariç); hücre kültürleri (değiştirilmiş olsun olmasın) · Tarım ve Orman Bakanlığı
- Applies to goods from
- all countries
- In force
- from 1 January 2026
- Legal act
- Tebliğ (Ürün Güvenliği ve Denetimi) 2026/5 (RG 31.12.2025, 33124 (4. Mükerrer)); değişik: RG 03.04.2026, RG 28.07.2026
- Import controlTedavide, korunmada veya teşhiste kullanılmak üzere hazırlanmış hayvan kanı · Tarım ve Orman Bakanlığı
- Applies to goods from
- all countries
- In force
- from 1 January 2026
- Legal act
- Tebliğ (Ürün Güvenliği ve Denetimi) 2026/5 (RG 31.12.2025, 33124 (4. Mükerrer)); değişik: RG 03.04.2026, RG 28.07.2026
Preferential rates by country
Same subheading in other tariffs
Türkiye lines: 3002.90
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.
- N320317 U.S. CBP
The tariff classification of glycerol stock of Escherichia coli (E. coli) from China
- N319434 U.S. CBP
The tariff classification of Recombinant Adeno-associated virus (AAV) packed for retail sale from China
- N319149 U.S. CBP
The tariff classification of ADSTILADRIN® (nadofaragene firadenovec-nrpl) in dosage form and a demonstration unit for Adstiladrin from Finland
- N319161 U.S. CBP
The tariff classification of Recombinant Lentivirus packed for retail sale from China, the United Kingdom and the European Union countries
- 600010730 HMRC
Human blood Use: clinical trials, laboratory research or diagnostic purposes Packaging: vial
- 600010289 HMRC
Avian blood that has been collected for diagnostic purposes. The blood can be from various species of birds. Normally 2 or 3 drops of blood are placed on blotting paper, submitted possibly with feather samples (these are being classified separately). They are for laboratory use only. Each…
17 rulings in total for this code
Legal notes
Notes
1. This chapter does not cover:
(a) foods or beverages (such as dietetic, diabetic or fortified foods, food supplements, tonic beverages and mineral waters), other than nutritional preparations for intravenous administration (Section IV);
(b) products, such as tablets, chewing gum or patches (transdermal systems), containing nicotine and intended to assist tobacco use cessation (heading 2404);
(c) plasters specially calcined or finely ground for use in dentistry (heading 2520);
(d) aqueous distillates or aqueous solutions of essential oils, suitable for medicinal uses (heading 3301);
(e) preparations of headings 3303 to 3307, even if they have therapeutic or prophylactic properties;
(f) soap or other products of heading 3401 containing added medicaments;
(g) preparations with a basis of plaster for use in dentistry (heading 3407);
(h) blood albumin not prepared for therapeutic or prophylactic uses (heading 3502); or
(ij) diagnostic reagents of heading 3822.
2. For the purposes of heading 3002, the expression ‘immunological products’ applies to peptides and proteins (other than goods of heading 2937) which are directly involved in the regulation of immunological processes, such as monoclonal antibodies (MAB), antibody fragments, antibody conjugates and antibody fragment conjugates, interleukins, interferons (IFN), chemokines and certain tumour-necrosis factors (TNF), growth factors (GF), hematopoietins and colony-stimulating factors (CSF).
3. For the purposes of headings 3003 and 3004 and of note 4(d) to this chapter, the following are to be treated:
(a) as unmixed products:
(1) unmixed products dissolved in water;
(2) all goods of Chapter 28 or 29; and
(3) simple vegetable extracts of heading 1302, merely standardised or dissolved in any solvent;
(b) as products which have been mixed:
(1) colloidal solutions and suspensions (other than colloidal sulphur);
(2) vegetable extracts obtained by the treatment of mixtures of vegetable materials; and
(3) salts and concentrates obtained by evaporating natural mineral waters.
4. Heading 3006 applies only to the following, which are to be classified in that heading and in no other heading of the nomenclature:
(a) sterile surgical catgut, similar sterile suture materials (including sterile absorbable surgical or dental yarns) and sterile tissue adhesives for surgical wound closure;
(b) sterile laminaria and sterile laminaria tents;
(c) sterile absorbable surgical or dental haemostatics; sterile surgical or dental adhesion barriers, whether or not absorbable;
(d) opacifying preparations for X-ray examinations and diagnostic reagents designed to be administered to the patient, being unmixed products put up in measured doses or products consisting of two or more ingredients which have been mixed together for such uses;
(e) placebos and blinded (or double-blinded) clinical trial kits for use in recognised clinical trials, put up in measured doses, even if they might contain active medicaments;
(f) dental cements and other dental fillings; bone reconstruction cements;
(g) first-aid boxes and kits;
(h) chemical contraceptive preparations based on hormones, on other products of heading 2937 or on spermicides;
(ij) gel preparations designed to be used in human or veterinary medicine as a lubricant for parts of the body for surgical operations or physical examinations or as a coupling agent between the body and medical instruments;
(k) waste pharmaceuticals, that is, pharmaceutical products which are unfit for their original intended purpose due to, for example, expiry of shelf life; and
(l) appliances identifiable for ostomy use, that is, colostomy, ileostomy and urostomy pouches cut to shape and their adhesive wafers or faceplates.
Subheading notes
1. For the purposes of subheadings 300213 and 300214, the following are to be treated:
(a) as unmixed products, pure products, whether or not containing impurities;
(b) as products which have been mixed:
(1) the products mentioned in (a) above dissolved in water or in other solvents;
(2) the products mentioned in (a) and (b) (1) above with an added stabiliser necessary for their preservation or transport; and
(3) The products mentioned in (a), (b) (1) and (b) (2) above with any other additive.
2. Subheadings 300360 and 300460 cover medicaments containing artemisinin (INN) for oral ingestion combined with other pharmaceutical active ingredients, or containing any of the following active principles, whether or not combined with other pharmaceutical active ingredients: amodiaquine (INN); artelinic acid or its salts; artenimol (INN); artemotil (INN); artemether (INN); artesunate (INN); chloroquine (INN); dihydroartemisinin (INN); lumefantrine (INN); mefloquine (INN); piperaquine (INN); pyrimethamine (INN) or sulfadoxine (INN).
In the Turkish Customs Tariff Schedule, 3002.90.30.00.00 is one of 2 lines under subheading 3002.90, human blood: other.
The statutory rate is free.
For the same subheading, the UK duty is free, the EU duty is free, the US duty is free, the Canada duty is free, the Mexico duty is 5%, the Brazil duty is 7.2%, the Argentina duty is 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.
Türkiye imported goods of subheading 3002.90 worth US$5m in 2024; the largest supplier was South Korea.
Questions and answers
What is the Türkiye import duty for GTİP code 3002.90.30.00.00?
The statutory rate in the Turkish Customs Tariff Schedule is free. Preferential rates for goods from agreement countries, anti-dumping duties and VAT are not included.
Where does Türkiye import these goods from?
For subheading 3002.90 as a whole, the largest supplier in 2024 was South Korea (US$2m), followed by the United States.
Typical products
Everyday names, not part of the legal text.