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Wieder® Inject+

by Societe Francaise D'instruments De Chirurgie 7 variants

Ref S001/0.3x25

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-FR-MF-00000416800037HJ Basic UDI-DI D-FR-MF-00000416800037HJUDI-DIDate30 Jun 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / Reference
S001/0.3x25
Primary DI / UDI-DI
D-FR-MF-00000416800037HJ
Basic UDI-DI
B-FR-MF-00000416800037HJ
EMDN Code
A010699 Dentistry needles and kits - other
Device Class
Class IIa
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
FR-MF-000004168

Other devices from Societe Francaise D'instruments De Chirurgie

See all devices from Societe Francaise D'instruments De Chirurgie →

Properties

  • Sterile
  • Administering Medicine

Other properties (9)

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