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Biocen 22 R

EUDAMED

Class A (EU MDR)

Ref CE 148IVDModel CE 146IVD

by Álvarez Redondo, S.A.

Identity

Trade Name
Biocen 22 R EUDAMED
Device Name
Biocen 22 EUDAMED
Model / Reference
CE 146IVD EUDAMED
CE 148IVD EUDAMED

Identifiers

Primary DI / UDI-DI
08436611980127 EUDAMED
Basic UDI-DI
843661198-IVD-BIO2-CE EUDAMED
EMDN Code
W02069005 REFRIGERATED CENTRIFUGES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Biocen 22 R by Álvarez Redondo, S.A. — 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

EUDAMED SRN
ES-MF-000000560

Sources (1)

  • EUDAMED cebed925-b3d6-433d-a1f2-8ead4313bc69 61 fields · synced Jun 19, 2026