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RPM Reinforced PTFE Mesh

by Osteogenics Biomedical, Inc. 17 variants

Ref RPM200PTCMEModel Titanium-Reinforced PTFE Mesh

Active European Union

CE MDD

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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-RPM200PTCMEDV Basic UDI-DI D-RPM200PTCMEDVUDI-DIDate19 Aug 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
RPM Reinforced PTFE Mesh, PTCM
Model / Reference
Titanium-Reinforced PTFE Mesh, RPM200PTCME
Primary DI / UDI-DI
D-RPM200PTCMEDV
Basic UDI-DI
B-RPM200PTCMEDV
EMDN Code
Q010301 Periodontal membranes
Device Class
Class IIb
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
US-MF-000004534
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Other devices from Osteogenics Biomedical, Inc.

See all devices from Osteogenics Biomedical, Inc. →

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