CN code 3002 14 00 Immunological products, mixed, not put up in measured doses or in forms or…
CN code 3002 14 00 covers immunological products, mixed, not put up in measured doses or in forms or packings for retail sale.
- Third-country duty
- 0 % (fri)
- EUDR
- Not in scope
- Level
- CN code
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Importing into the EU
TARIC codes (10 digits): 1
Goods that have been classified here
Examples from the EU database of Binding Tariff Information (BTI). A ruling binds only its holder and many have expired — read them as guidance, not as a decision for your product.
PEMBROLIZUMAB DRUG SUBSTANCE (FINAL FORMULATED BULK - FFB) THE PRODUCT IS USED FOR PHARMACEUTICAL (BIOLOGIC IMMUNOLOGICAL). THE PRODUCT IS PRODUCED IN BULK AS A FROZEN LIQUID AND HAS A COLOURLESS TO PALE YELLOW APPEARANCE.
MK-6072 (BEZLOTOXUMAB) FFB. (FINAL FORMULATED BULK). FOR PHARMACEUTICAL (BIOLOGIC/IMMUNOLOGICAL DRUG SUBSTANCE)USE. IT IS BEING IMPORTED IN BULK AS A FROZEN LIQUID. IT IS COLOURLESS TO PALE YELLOW IN APPEARANCE.
PEMBROLIZUMAB FFB (FINAL FORMULATED BULK) FOR PHARMACEUTICAL (BIOLOGIC IMMUNOLOGICAL DRUG SUBSTANCE) USE. IMPORTED IN BULK AS A FROZEN LIQUID. IT IS COLOURLESS TO PALE YELLOW IN APPEARANCE.
MK-1308 FFB (FINAL FORMULATED BULK) FOR PHARMACEUTICAL (BIOLOGIC/IMMUNOLOGICAL DRUG SUBSTANCE)USE. THE PRODUCT IS BEING IMPORTED IN BULK AS A FROZEN LIQUID. THE PRODUCT IS COLOURLESS TO PALE YELLOW IN APPEARANCE.
MEDICAMENT WHICH IS PUT TO TREAT RHEUMATOID ARTHRITIS : ITS ACTIVE SUBSTANCE HAS IMMUNOLOGICAL PROPERTIES. PRODUCT IS MIXED AND NOT PUT UP IN MEASURED DOSES OR IN FORMS OR PACKINGS FOR RETAIL SALE
THE IMMUNOASSAY DIAGNOSTICS REAGENTS AT BECKMAN COULTER IN A CHEMICAL REACTION TO DETECT ANALYSE OR PRODUCE ANOTHER SUBSTANCE WHICH INDICATES THE PRESENT OF A SPECIAL CONDITION. BECKMAN PRODUCE A WIDE RANGE OF REAGENTS. THESE ARE ALL USED 'IN VITRO' WHICH MEANS A REAGENT IS USED FOR THE EXAMINATION OF BLOOD AND TISSUE EXTRACTED FROM THE HUMAN BODY, SOLELY OR PRINCIPALLY FOR THE PURPOSE OF…
(ENB-0040), ALSO KNOWN AS STRENSIQ, IS A TARGETED ENZYME REPLACEMENT THERAPY DESIGNED TO ADDRESS THE UNDERLYING CAUSE OF HYPOPHOSPHATASIA (HPP) BY NORMALIZING THE GENETICALLY DEFECTIVE METABOLIC PROCESS, AND PREVENTING OR REVERSING THE SEVERE AND LIFE-THREATENING COMPLICATIONS OF LIFE-LONG DYSREGULATED MINERAL METABOLISM. ITS MAIN COMPONENT ASFOTASE ALFA IS A RECOMBINANT FUSION PROTEIN COMPRISED…
SOLIRIS IS A THERAPY SPECIFICALLY TESTED AND APPROVED FOR THE TREATMENT OF PATIENTS WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA (PNH), AN ULTRA-RARE, LIFE-THREATENING BLOOD DISORDER. SOLIRIS HAS BEEN APPROVED FOR THE TREATMENT OF PATIENTS WITH PNH IN NEARLY 50 COUNTRIES WORLDWIDE. SOLIRIS 300 MG/30ML IS A FORMULATION OF ECULIZUMAB WHICH IS A RECOMBINANT HUMANIZED MONOCLONAL IGG2/4;κ ANTIBODY…
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Describe the product in your own words and Klassio suggests a CN code with reasoning, duty and EUDR status.