Skip to content

DRD Blood

by FertiPro

Ref DRDB_1

DRD Blood (DRDB_1) is a Class A device made by FertiPro, registered in EUDAMED on 24 Mar 2026 (Basic UDI-DI 5411967DRDB1TD), 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 Number5411967DRDB1TD Basic UDI-DI 05411967007394UDI-DIDate24 Mar 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / reference
DRDB_1
Primary DI / UDI-DI
05411967007394
Basic UDI-DI
5411967DRDB1TD
Direct marketing DI
05411967007394
EMDN code
W050101010201 Blood collection, tubes with additives or serum separator
Device class
Class A
EU registration type
Standard device
EU market of registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000000313

Similar devices in this category

Other devices filed under BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR.

Other devices from FertiPro

See all devices from FertiPro →

Properties

  • Professional testing
Other properties (12, all answered No)