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Reduction support base

by Nouvag AG 5 variants

Ref 19887

Reduction support base (19887) is a Class I device made by Nouvag AG, registered in EUDAMED on 19 Oct 2026 (Basic UDI-DI ++ENOU100033LL), 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, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 7 Nov 2026.

Regulatory status

as of registry sync 7 Nov 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number++ENOU100033LL Basic UDI-DI +ENOU198871.UDI-DIDate19 Oct 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  • Withdrawn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

Model / reference
19887
Primary DI / UDI-DI
+ENOU198871.
Basic UDI-DI
++ENOU100033LL
EMDN code
L0103 Dermotomes and blades, reusable
Device class
Class I
EU registration type
Standard device
EU market of registration
Germany

Manufacturer details

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

Similar devices in this category

Other devices filed under DERMOTOMES AND BLADES, REUSABLE.

Other devices from Nouvag AG

See all devices from Nouvag AG →

Properties

  • Sterilise before use
Other properties (13, all answered No)