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nopa

by nopa instruments Medizintechnik GmbH 1,000+ variants

Part of a family of 29 devices: see the family page

Ref KD 668/22Model Anoskop

nopa (KD 668/22) is a Class I device made by nopa instruments Medizintechnik GmbH, registered in EUDAMED on 5 Jun 2026 (Basic UDI-DI 404953800000059BH), active as of 25 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number404953800000059BH Basic UDI-DI 14049538081603UDI-DIDate5 Jun 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
Anoskop, KD 668/22
Primary DI / UDI-DI
14049538081603
Basic UDI-DI
404953800000059BH
Direct marketing DI
14049538081603
EMDN code
L040902 Rectal and anal spreaders, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005613

Similar devices in this category

Other devices filed under ABDOMINAL SURGERY DILATORS AND SPREADERS, REUSABLE.

Other devices from nopa instruments Medizintechnik GmbH

  • nopa

    Class IIb

  • nopa

    Class IIa

  • nopa

    Class I

  • nopa

    Class I

See all devices from nopa instruments Medizintechnik GmbH →

Properties

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