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Omniplast

by Paul Hartmann AG 15 variants

Ref 900504Model 1681

Omniplast (900504) is a Class I device made by Paul Hartmann AG, registered in EUDAMED on 4 Oct 2026 (Basic UDI-DI 40495001681KX), 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 Number40495001681KX Basic UDI-DI 04052199237534UDI-DIDate4 Oct 2026RegisteredStatusActive EUDAMED: not on the EU market

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  • Withdrawn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
1681, 900504
Primary DI / UDI-DI
04052199237534
Basic UDI-DI
40495001681KX
EMDN code
M050199 Surgical plasters - other
Device class
Class I
EU registration type
Standard device

Manufacturer details

EUDAMED SRN
DE-MF-000005861

Similar devices in this category

Other devices filed under SURGICAL PLASTERS.

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Properties

Other properties (14, all answered No)