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A17362-75

by Foosin Medical Supplies Inc., Ltd.

Ref A17362-75Model PGLA

A17362-75 is a Class III device made by Foosin Medical Supplies, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI B-06941813628224), 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-06941813628224 Basic UDI-DI 06941813628224UDI-DIDate28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
PGLA, A17362-75
Primary DI / UDI-DI
06941813628224
Basic UDI-DI
B-06941813628224
Direct marketing DI
06941813628224
EMDN code
H010101020202 Polyglycolic with lactic acid multifilament with needle for video surgery
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000006957
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

Similar devices in this category

Other devices filed under POLYGLYCOLIC WITH LACTIC ACID MULTIFILAMENT.

Other devices from Foosin Medical Supplies, Inc.

See all devices from Foosin Medical Supplies, Inc. →

Properties

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