Skip to content

Ic 6955-42

by aap Implantate AG

Ref IC 6955-42Model Instrument

Ic 6955-42 is a Class I device made by Aap Implantate AG, registered in EUDAMED on 29 May 2026 (Basic UDI-DI 40424090079HL), active as of 7 Nov 2026.

Active European Union

CE MDR

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/MDR Number40424090079HL Basic UDI-DI 04042409453427UDI-DIDate29 May 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Instrument, IC 6955-42
Primary DI / UDI-DI
04042409453427
Basic UDI-DI
40424090079HL
EMDN code
V0402 Clinical use trays and bowls
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005994

Other devices from Aap Implantate AG

See all devices from Aap Implantate AG →

Properties

  • Sterilise before use
  • Reusable
Other properties (12, all answered No)