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AB1302-75

by Foosin Medical Supplies Inc., Ltd.

Ref AB1302-75Model PGLA

AB1302-75 is a Class III device made by Foosin Medical Supplies Inc., Ltd., registered in EUDAMED on 22 Sep 2026 (Basic UDI-DI B-06942339397762), active as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06942339397762 Basic UDI-DI 06942339397762UDI-DIDate22 Sep 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
PGLA, AB1302-75
Primary DI / UDI-DI
06942339397762
Basic UDI-DI
B-06942339397762
EMDN code
H010101020201, H010101020202
Device class
Class III
EU registration type
Legacy device (under a directive)
EU market of registration
Lithuania

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 WITH NEEDLE FOR OPEN SURGERY.

Other devices from Foosin Medical Supplies Inc., Ltd.

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Properties

  • Supplied sterile
  • Implantable
Other properties (10, all answered No)