Skip to content

GraftR3®

by Advanced Medical Solutions (Nantes) SAS

Ref GR1801LY05

Active European Union

CE MDR

Valid until

24 Jun 2031

CE MDR 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/MDR Number3700501821306013D Basic UDI-DI 03700501814355UDI-DIDate3 Jul 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

France
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

EU market availability

Made available in 1 country, as listed in EUDAMED:

Declared by the manufacturer in EUDAMED for this device version; may not cover every market.

  • France since 3 Jul 2026

Last checked 28 Oct 2026.

Specification

EUDAMED

Device Name
Freeze Dried Bone Scaffold
Model / Reference
GR1801LY05
Primary DI / UDI-DI
03700501814355
Basic UDI-DI
3700501821306013D
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000016065

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