Disposable Vacuum Blood Tube

by Zhejiang Gongdong Medical Technology Co., Ltd., 123 variants

Ref GD030SPModel Disposable Vacuum Blood Tube(Potassium oxalate+Sodium fluoride)

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	Number6947462411111129LZ Basic UDI-DI 06947462493701UDI-DI	Date22 Sep 2022Registered	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Withdrawn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: Disposable Vacuum Blood Tube(Potassium oxalate+Sodium fluoride)
Model / Reference: Disposable Vacuum Blood Tube(Potassium oxalate+Sodium fluoride), GD030SP

Primary DI / UDI-DI: 06947462493701
Basic UDI-DI: 6947462411111129LZ
EMDN Code: W050101010201 Blood collection, tubes with additives or serum separator

Device Class: Class A
EU market of registration: Germany

Manufacturer details

EUDAMED SRN: CN-MF-000005694
Authorised representative: Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

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Properties

Sterile
Professional Testing
Surgical Instrument

Other properties (8)