Skip to content

Duraguard medium

by Nouvag AG

Ref 1923nou

Duraguard medium (1923nou) is a Class IIa device made by Nouvag AG, registered in EUDAMED on 9 Jul 2026 (Basic UDI-DI B-+ENOU1923NOU9I), active as of 25 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-+ENOU1923NOU9I Basic UDI-DI Date9 Jul 2026RegisteredStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Active

Specification

EUDAMED

Model / reference
1923nou
Primary DI / UDI-DI
+ENOU1923NOU9I, +ENOU1923NOU1A
Basic UDI-DI
B-+ENOU1923NOU9I, B-+ENOU1923NOU1A
EMDN code
Z12100980 Instruments for motorised neurosurgery systems - hardware accessories
Device class
Class IIa
EU registration type
Legacy device (under a directive)
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
CH-MF-000018882
Authorised representative
Nouvag Dental- und Medizintechnik GmbH DE-AR-000005643

Similar devices in this category

Other devices filed under INSTRUMENTS FOR MOTORISED NEUROSURGERY SYSTEMS - HARDWARE ACCESSORIES.

Other devices from Nouvag AG

See all devices from Nouvag AG →

Properties

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