Skip to content

Aiguille non stérile réutilisable

by Thread & Lift

Ref 030_01_2200 / 030_01_2300 / 030_01_2400 / 030_01_2500 / 030_01_2600

Active European Union

CE MDD

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 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-030_01_2200EK Basic UDI-DI D-030_01_2200EKUDI-DIDate14 Jun 2022RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
030_01_2200 / 030_01_2300 / 030_01_2400 / 030_01_2500 / 030_01_2600
Primary DI / UDI-DI
D-030_01_2200EK
Basic UDI-DI
B-030_01_2200EK
EMDN Code
L0202 Suture needles, reusable
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
BE-MF-000010385

Other devices from Thread & Lift

Properties

  • Reusable

Other properties (10)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No