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ClinRep® Complete Kit for 25-OH-Vitamin D2/D3 in Plasma and Serum by UHPLC

by RECIPE Chemicals + Instruments GmbH

Ref 35100, 35000

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 Number4049195B35X00C4 Basic UDI-DI Date7 Apr 2025RegisteredStatusActive

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  • Withdrawn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

Trade Name
ClinRep® Complete Kit for 25-OH-Vitamin D2/D3 in Plasma and Serum by UHPLC
ClinRep® Complete Kit for 25-OH-Vitamin D2/D3 in Plasma and Serum
Device Name
25-Hydroxy-Vitamin D2/D3 in Plasma and Serum
Model / Reference
35100, 35000
Primary DI / UDI-DI
04049195351005, 04049195350008
Basic UDI-DI
4049195B35X00C4
Direct Marketing DI
04049195351005
04049195350008
EMDN Code
W01010499 Multiple clin. chem lab reagents - other
Device Class
Class B
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000032553

From the manufacturer

Manufacturer's product page: Complete Kits LC-MS/MS

Other devices from RECIPE Chemicals + Instruments GmbH

See all devices from RECIPE Chemicals + Instruments GmbH →

Properties

  • Reagent
  • Professional Testing

Other properties (9)

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