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Magnus 22

EUDAMED

Class A (EU MDR)

Ref CE 231IVDModel CE 230IVD

by Álvarez Redondo, S.A.

Identity

Trade Name
Magnus 22 EUDAMED
Device Name
Magnus 22 EUDAMED
Model / Reference
CE 230IVD EUDAMED
CE 231IVD EUDAMED

Identifiers

Primary DI / UDI-DI
08436611980684 EUDAMED
Basic UDI-DI
843661198-IVD-MGN2-FL EUDAMED
EMDN Code
W02069003 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

Category: General-purpose centrifuge IVD

Magnus 22 by Álvarez Redondo, S.A. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-purpose centrifuge IVD.

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 61e8292d-927e-4086-b23d-8b23a0f092d8 61 fields · synced Jun 19, 2026