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ClinMass® Internal Standard, lyophil., for Immunosuppressants (d₁₂-Cyclosporine A, ¹³Cd₂-Tacrolimus, ¹³Cd₃-Sirolimus, ¹³C₂d₄-Everolimus)

by RECIPE Chemicals + Instruments GmbH

Ref MS1312

Active European Union

CE IVDD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-MS1312AR Basic UDI-DI D-MS1312ARUDI-DIDate7 May 2026RegisteredStatusActive

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  • Withdrawn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/IVDD Active

Specification

EUDAMED

Device Name
Internal Standard for Immunosuppressants (d₁₂-Cyclosporine A, ¹³Cd₂-Tacrolimus, ¹³Cd₃-Sirolimus, ¹³C₂d₄-Everolimus)
Model / Reference
MS1312
Primary DI / UDI-DI
D-MS1312AR
Basic UDI-DI
B-MS1312AR
EMDN Code
W0101050303 Aqueous standards (cc)
Device Class
Class IVD General
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000032553

From the manufacturer

Manufacturer's product page: Internal Standards

Other devices from RECIPE Chemicals + Instruments GmbH

See all devices from RECIPE Chemicals + Instruments GmbH →

Properties

  • Reagent
  • Professional Testing

Other properties (8)

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