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Sterile Extraperitoneal Non-Resorbable Parietal reinforcement implants

by Cousin Biotech 61 variants

Ref VCBPMF128UModel PREMIUM

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-03760185575003 Basic UDI-DI 03760185575003UDI-DIDate12 Jun 2025RegisteredStatusActive

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  • Withdrawn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
Sterile Extraperitoneal Non-Resorbable Parietal reinforcement implants
Model / Reference
PREMIUM, VCBPMF128U
Primary DI / UDI-DI
03760185575003
Basic UDI-DI
B-03760185575003
EMDN Code
P900202 Polypropylene surgical meshes
Device Class
Class IIb
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001179

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See all devices from Cousin Biotech →

Properties

  • Sterile
  • Implantable

Other properties (9)

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