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DRD Blood

EUDAMED

Class A (EU MDR)

Ref DRDB_1

by FertiPro

Identity

Trade Name
DRD Blood EUDAMED
Device Name
DRD Blood EUDAMED
Model / Reference
DRDB_1 EUDAMED

Identifiers

Primary DI / UDI-DI
05411967007394 EUDAMED
Basic UDI-DI
5411967DRDB1TD EUDAMED
Direct Marketing DI
05411967007394 EUDAMED
EMDN Code
W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

DRD Blood by FertiPro — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
FertiPro
EUDAMED SRN
BE-MF-000000313

Sources (1)

  • EUDAMED 7b7ac89e-021a-4439-b846-d328fabf07f2 61 fields · synced Jun 18, 2026