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Novosyn

by B. Braun Surgical, S.A. 122 variants

Ref C0068291N1

Active European Union

CE MDR

Valid until

28 Apr 2029

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 Number40392390000018302P Basic UDI-DI 04046955556069UDI-DIDate18 Sep 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / Reference
C0068291N1
Primary DI / UDI-DI
04046955556069
Basic UDI-DI
40392390000018302P
Unit of Use DI
04046955549696
EMDN Code
H010101020201 Polyglycolic with lactic acid multifilament with needle for open surgery
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
ES-MF-000002083

Other devices from B. Braun Surgical, S.A.

  • Novosyn

    Class III

  • Histoacryl Flexible

    Class IIa

  • Novosyn

    Class III

  • Novosyn

    Class III

  • Novosyn

    Class III

  • Novosyn

    Class III

See all devices from B. Braun Surgical, S.A. →

Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

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