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Drdp

by FertiPro 2 variants

Ref DRDP_0002

Drdp (DRDP_0002) is a Class A device made by FertiPro, registered in EUDAMED on 6 Jan 2025 (Basic UDI-DI 5411967DRDP1UP), active as of 22 Oct 2026.

Active European Union

CE IVDR

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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number5411967DRDP1UP Basic UDI-DI 05411967007127UDI-DIDate6 Jan 2025RegisteredStatusActive

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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / reference
DRDP_0002
Primary DI / UDI-DI
05411967007127
Basic UDI-DI
5411967DRDP1UP
Direct marketing DI
05411967007127
EMDN code
W0104010203 Transport media
Device class
Class A
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000000313

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Properties

  • Contains animal tissues or cells
  • Professional testing
Other properties (11, all answered No)