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Vacutainer

EUDAMED

Class A (EU MDR)

Ref 368521

by Becton, Dickinson and Company

Identity

Trade Name
Vacutainer EUDAMED
Device Name
BD Vacutainer® Fluoride Blood Collection Tubes EUDAMED
Model / Reference
368521 EUDAMED

Identifiers

Primary DI / UDI-DI
30382903685210 EUDAMED
Basic UDI-DI
038290NWWJFZVQRU EUDAMED
Unit of Use DI
00382903685219 EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Vacutainer by Becton, Dickinson and Company — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
US-MF-000019182
Authorised Representative
Becton Dickinson Ireland Limited IE-AR-000007610

Sources (1)

  • EUDAMED 00fff8bc-c4c5-46f4-9c80-111556c37974 61 fields · synced Oct 9, 2026