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ParieteneTM

by Sofradim Production 5 variants

Ref PPL2020

ParieteneTM (PPL2020) is a Class III device made by Sofradim Production, registered in EUDAMED on 20 Jul 2026 (Basic UDI-DI 0763000B000103374), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0763000B000103374 Basic UDI-DI 10884521179097UDI-DIDate20 Jul 2026RegisteredStatusActive

Official records

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 729726 Active Reissued Removed from EUDAMED

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    29 Jun 2026
    Expires
    28 Jun 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
ParieteneTM Lightweight Mesh
Model / reference
PPL2020
Primary DI / UDI-DI
10884521179097
Basic UDI-DI
0763000B000103374
EMDN code
P900202 Polypropylene surgical meshes
Device class
Class III
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000012211

Similar devices in this category

Other devices filed under POLYPROPYLENE SURGICAL MESHES.

Other devices from Sofradim Production

See all devices from Sofradim Production →

Properties

  • Supplied sterile
  • Implantable
Other properties (12, all answered No)