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V53193B-75

by Foosin Medical Supplies Inc., Ltd.

Ref V53193B-75Model SUPRAMID NYLON

Active European Union

CE MDR

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number69418136NA-suturesIIbV89 Basic UDI-DI 06941813680116UDI-DIDate26 May 2026RegisteredStatusActive

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  • Withdrawn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/MDR Active

Specification

EUDAMED

Model / Reference
SUPRAMID NYLON, V53193B-75
Primary DI / UDI-DI
06941813680116
Basic UDI-DI
69418136NA-suturesIIbV89
Direct Marketing DI
06941813680116
EMDN Code
H010201010101 Polyamide monofilament with needle
Device Class
Class IIb
EU market of registration
Lithuania

Manufacturer details

EUDAMED SRN
CN-MF-000006957
Authorised representative
MedNet EC-REP C III GmbH DE-AR-000011196

Other devices from Foosin Medical Supplies, Inc.

See all devices from Foosin Medical Supplies, Inc. →

Properties

  • Sterile
  • Implantable
  • Sutures

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