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Digicen 22R

EUDAMED

Class A (EU MDR)

Ref CE 260IVDModel CE 257IVDRef CE 259IVD

by Álvarez Redondo, S.A.

Identity

Trade Name
Digicen 22R EUDAMED
Device Name
Digicen 22 EUDAMED
Model / Reference
CE 257IVD EUDAMED
CE 260IVD EUDAMED
CE 259IVD EUDAMED

Identifiers

Primary DI / UDI-DI
08436611981155 EUDAMED
08436611981148 EUDAMED
Basic UDI-DI
843661198-IVD-DIG2-BU 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

Digicen 22R 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 (2)

  • EUDAMED acc61154-ebbc-495e-bad1-92057501d8e3 61 fields · synced Jul 16, 2026
  • EUDAMED 72e1f47e-1527-4492-9248-11e10c1d4134 61 fields · synced May 16, 2026