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Q-NADMED Blood NAD+ and NADH Assay kit_S

by NADMED Oy

Ref IVD_001_S, IVD_001

Active European Union

CE IVDR CE IVDD

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 NumberB-06429830166627 Basic UDI-DI Date19 Mar 2026RegisteredStatusActive
European UnionCE/IVDD NumberB-06429830166627 Basic UDI-DI Date19 Mar 2026RegisteredStatusActive

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  • Withdrawn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, CE/IVDD Active

Specification

EUDAMED

Trade Name
Q-NADMED Blood NAD+ and NADH Assay kit_S
Q-NADMED Blood NAD+ and NADH Assay kit
Device Name
Q-NADMED Blood
Q-NADMED Blood NAD+ and NADH Assay kit - SMALL
Model / Reference
IVD_001_S, IVD_001
Primary DI / UDI-DI
06429830166627, 06429830166603
Basic UDI-DI
B-06429830166627, B-06429830166603, 6429830166614141354NT
Direct Marketing DI
06429830166627
EMDN Code
W01010404 Multiple parameters (mix of all) - clin. chem lab r.
Device Class
Class IVD General
Class B
EU market of registration
Finland

Manufacturer details

EUDAMED SRN
FI-MF-000023612

Properties

  • Microbial Substances
  • Reagent
  • Professional Testing

Other properties (8)

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