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Ifabond®

by Advanced Medical Solutions (France) SAS 3 variants

Ref IB

Active European Union

CE MDR

Valid until

2 Jul 2029

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number39929 Date15 Sep 2026IssuedStatusActive expires 2 Jul 2029

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 39929 Active Supplemented

    Technical documentation EU MDR

    Certifier
    GMED SAS 0459
    Issued
    15 Sep 2026
    Expires
    2 Jul 2029
    Reason
    Other

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Surgical and tissue glue for internal use
Model / Reference
IB
Primary DI / UDI-DI
13661522038519
Basic UDI-DI
3661522DTCO0101LY
EMDN Code
H90010102, H900305, H900399
Device Class
Class III
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

Other properties (11)

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