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Serafit®

by SERAG-WIESSNER GmbH & Co. KG 16 variants

Ref 7Z401700

Serafit® (7Z401700) is a Class III device made by SERAG-WIESSNER GmbH & Co. KG, registered in EUDAMED on 27 Oct 2026 (Basic UDI-DI B-14044973133610), active as of 7 Nov 2026.

Active European Union

CE MDD

Valid until

No date given

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

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-14044973133610 Basic UDI-DI 14044973133610UDI-DIDate27 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Device name
PGA suture material
Model / reference
7Z401700
Primary DI / UDI-DI
14044973133610
Basic UDI-DI
B-14044973133610
EMDN code
H010101020103 Polyglycolic acid multifilament without needle
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000006422

Similar devices in this category

Other devices filed under POLYGLYCOLIC ACID MULTIFILAMENT WITHOUT NEEDLE.

Other devices from SERAG-WIESSNER GmbH & Co. KG

See all devices from SERAG-WIESSNER GmbH & Co. KG →

Properties

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