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blood collection tube

by Weihai Optech Medical Instruments Co., Ltd

Ref VN08101PModel No additive 13*75 1ml

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number697779522VN08101P95 Basic UDI-DI 06977795221016UDI-DIDate19 Sep 2024RegisteredStatusActive EUDAMED: not on the EU market

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

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
blood collection tube
Model / Reference
No additive 13*75 1ml, VN08101P
Primary DI / UDI-DI
06977795221016
Basic UDI-DI
697779522VN08101P95
EMDN Code
W050101010202 Blood collection, tubes without additives or serum separator
Device Class
Class A

Manufacturer details

EUDAMED SRN
CN-MF-000031847
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Properties

  • Sterile
  • New Device

Other properties (9)

  • 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