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Ruisku-neulasetti STOP

by Oy Medifon Ab (a wholesaler of medicines)

Ref 6418086999806

Withdrawn Withdrawn in European Union. No longer placed on the EU market.

Was authorized under CE MDR, withdrawn

Ended

Withdrawn

Date not published (CE MDR)

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/MDR Number6418086MF1E9 Basic UDI-DI 06418086999806UDI-DIDate9 Aug 2023RegisteredStatusWithdrawn No longer placed on the EU market

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  • Withdrawn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European Union — CE/MDR Withdrawn

Specification

EUDAMED

Model / Reference
6418086999806
Primary DI / UDI-DI
06418086999806
Basic UDI-DI
6418086MF1E9
EMDN Code
A99 Devices for administration, withdrawal and collection - other
Device Class
Class IIa
Medical Purpose
Huumeenkäyttäjien terveyshaittojen ehkäisy ja vähentäminen.

Manufacturer details

EUDAMED SRN
FI-PR-000036310

Properties

Other properties (1)

  • Sterile: No