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PVDF Suture material

by SERAG-WIESSNER GmbH & Co. KG

Ref LO05171254

Active European Union

CE MDR

Valid until

10 Aug 2031

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier mdc medical device certification 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 NumberD1453500025 Date11 Aug 2026IssuedStatusActive expires 10 Aug 2031

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • D1453500025 Active

    Technical documentation EU MDR

    Certifier
    mdc medical device certification GmbH 0483
    Issued
    11 Aug 2026
    Expires
    10 Aug 2031

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
PVDF Suture material
Model / Reference
LO05171254
Primary DI / UDI-DI
04044973106808
Basic UDI-DI
4044973CE12UA
EMDN Code
H010201010601 Polyvinylidene fluoride and derivatives monofilament with needle
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006422

Other devices from SERAG-WIESSNER GmbH & Co. KG

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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