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Neoss® Guide Kit System Box

by Neoss AB

Part of a family of 8 devices: see the family page

Ref 51241

Neoss® Guide Kit System Box (51241) is a Class I device made by Neoss AB, registered in EUDAMED on 12 May 2026 (Basic UDI-DI 506044033N0028N7), active as of 24 Oct 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506044033N0028N7 Basic UDI-DI 05060440337505UDI-DIDate12 May 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device name
Storage
Model / reference
51241
Primary DI / UDI-DI
05060440337505
Basic UDI-DI
506044033N0028N7
Direct marketing DI
05060440337505
EMDN code
P01020180 Dental implants - accessories
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
SE-MF-000022321

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Properties

Other properties (14, all answered No)