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Vacuum Blood Collection Tube

EUDAMED

Class A (EU MDR)

Ref 6213Model blood glucose test tube, heparin sodium/fluoride

by Jiangsu KangJian Medical Apparatus Co., Ltd.

Identity

Device Name
Vacuum Blood Collection Tube EUDAMED
Model / Reference
blood glucose test tube, heparin sodium/fluoride EUDAMED
6213 EUDAMED

Identifiers

Primary DI / UDI-DI
26953211362130 EUDAMED
Basic UDI-DI
69532113VBCTHSFL5Y EUDAMED
Unit of Use DI
06953211362136 EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Vacuum Blood Collection Tube by Jiangsu KangJian Medical Apparatus Co., Ltd. — 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
CN-MF-000018938
Authorised Representative
Zoustech S.L. ES-AR-000002008

Sources (1)

  • EUDAMED 1b114402-f195-4046-87ab-fbf2b002262b 61 fields · synced Oct 6, 2026