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Mission® Cholesterol Monitoring System

by ACON Laboratories, Inc.

Ref C111-2011-101Model CCM-111

Active European Union

CE IVDR

Valid until

4 Aug 2031

CE IVDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier TÜV SÜD Product Service GmbH

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 Number68260799999901003Y Basic UDI-DI 00682607612345UDI-DIDate6 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Specification

EUDAMED

Model / Reference
CCM-111, C111-2011-101
Primary DI / UDI-DI
00682607612345
Basic UDI-DI
68260799999901003Y
EMDN Code
V010401, W010106010802, W0101060109, W0201069080
Device Class
Class C
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000023913
Authorised representative
MDSS GmbH DE-AR-000005430

Other devices from Acon Laboratories, Inc.

See all devices from Acon Laboratories, Inc. →

Properties

  • Microbial Substances
  • Reagent
  • Self Testing
  • Near-Patient Testing
  • Professional Testing
  • Surgical Instrument

Other properties (5)

  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Companion Diagnostics: No
  • New Device: No