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Glactime®

by Advanced Medical Solutions (France) SAS

Ref 39G40F

Active European Union

CE MDR

Valid until

16 Aug 2028

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier GMED SAS

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/MDR Number3661522DTSU1801WU Basic UDI-DI 03661522037188UDI-DIDate20 Aug 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 39383 Active Amended

    Technical documentation EU MDR

    Certifier
    GMED SAS 0459
    Issued
    22 Jul 2026
    Expires
    16 Aug 2028
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
39G40F
Primary DI / UDI-DI
03661522037188
Basic UDI-DI
3661522DTSU1801WU
EMDN Code
H010101020201, H010101020202
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000666

Other devices from Advanced Medical Solutions (France) SAS

See all devices from Advanced Medical Solutions (France) SAS →

Properties

  • Sterile
  • Implantable
  • Animal Tissues

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No