Vacuum Blood Collection Tube

by Jiangsu KangJian Medical Apparatus Co., Ltd. 215 variants

Ref 6023Model no additive tube

Active European Union

CE IVDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/IVDR	Number69532113VBCTNoneFE Basic UDI-DI 26953211360235UDI-DI	Date15 May 2023Registered	StatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name: Vacuum Blood Collection Tube
Model / Reference: no additive tube, 6023

Primary DI / UDI-DI: 26953211360235
Basic UDI-DI: 69532113VBCTNoneFE
Unit of Use DI: 06953211360231
EMDN Code: W050101010202 Blood collection, tubes without additives or serum separator

Device Class: Class A
EU market of registration: Spain

Manufacturer details

EUDAMED SRN: CN-MF-000018938
Authorised representative: Zoustech S.L. ES-AR-000002008

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Properties

Sterile

Other properties (10)

Human Tissues: No
Animal Tissues: No
Microbial Substances: No
Reagent: No
Self Testing: No
Near-Patient Testing: No
Professional Testing: No
Companion Diagnostics: No
Surgical Instrument: No
New Device: No