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Anti-M for card method monoclonal, mouse Clone: LM110/140

by ANTITOXIN GmbH 2 variants

Ref 01.179-05

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number4250861801.179KY Basic UDI-DI 04250861807423UDI-DIDate6 May 2024RegisteredStatusActive

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  • Withdrawn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
Anti-M for card method monoclonal, mouse (Grifols) Clone: LM110/140
Model / Reference
01.179-05
Primary DI / UDI-DI
04250861807423
Basic UDI-DI
4250861801.179KY
EMDN Code
W01030399 Immunohaematology (blood grouping) tests - other
Device Class
Class C
EU market of registration
Austria

Manufacturer details

EUDAMED SRN
DE-MF-000008156

Other devices from ANTITOXIN GmbH

See all devices from ANTITOXIN 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