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Vacuum Blood Collection Tube

EUDAMED

Class A (EU MDR)

Ref 6333Model PPT tube, K3-EDTA/gel

by Jiangsu KangJian Medical Apparatus Co., Ltd.

Identity

Device Name
Vacuum Blood Collection Tube EUDAMED
Model / Reference
PPT tube, K3-EDTA/gel EUDAMED
6333 EUDAMED

Identifiers

Primary DI / UDI-DI
26953211363335 EUDAMED
Basic UDI-DI
69532113VBCTK3EGel5K EUDAMED
Unit of Use DI
06953211363331 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 dec5a34f-61f2-4b73-a0cd-7fa56c764583 61 fields · synced Jun 18, 2026