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Blood Collection Tube - Sodium Heparin (Vacuum) (2ML)(PET)

by Nasmed Diagnostic Private Limited 12 variants

Ref Blood Collection Tube - Sodium Heparin (Vacuum) (9ML)(PET)

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, self-declared

Class I: no certifier involved

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

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number890617952NSHTW Basic UDI-DI 08906179520597UDI-DIDate11 Jun 2024RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Device Name
Blood Collection Tube - Sodium Heparin (Vacuum) (2ML)(PET)
Model / Reference
Blood Collection Tube - Sodium Heparin (Vacuum) (9ML)(PET)
Primary DI / UDI-DI
08906179520597
Basic UDI-DI
890617952NSHTW
Direct Marketing DI
08906179520597
EMDN Code
W050101010201 Blood collection, tubes with additives or serum separator
Device Class
Class A
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
IN-MF-000039587
Authorised representative
AF Pharma Service Europe SL ES-AR-000018076

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See all devices from Nasmed Diagnostic Private Limited →

Properties

  • Professional Testing

Other properties (10)

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