Skip to content

N23243-90

by Foosin Medical Supplies Inc., Ltd.

Ref N23243-90Model Nylon

N23243-90 is a Class IIb device made by Foosin Medical Supplies, Inc., registered in EUDAMED on 28 Oct 2026 (Basic UDI-DI B-06941813664673), 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-06941813664673 Basic UDI-DI Date28 Oct 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
Nylon, N23243-90
Primary DI / UDI-DI
06941813664673, 06942339395294
Basic UDI-DI
B-06941813664673, B-06942339395294
Direct marketing DI
06941813664673
06942339395294
EMDN code
H010201010101 Polyamide monofilament with needle
Device class
Class IIb
EU registration type
Legacy device (under a directive)
EU market of registration
Spain

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 POLYAMIDE MONOFILAMENT WITH NEEDLE.

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)