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Rotofix 32 A

EUDAMED

Class A (EU MDR)

Ref 1206

by Andreas Hettich GmbH

Identity

Trade Name
ROTOFIX 32 A EUDAMED
ROTOFIX 32A, 208-240V 50-60Hz EUDAMED
Device Name
ROTOFIX 32 A EUDAMED
Model / Reference
1206 EUDAMED

Identifiers

Primary DI / UDI-DI
04050674039109 EUDAMED
Basic UDI-DI
040506740100129P EUDAMED
Direct Marketing DI
04050674039109 EUDAMED
EMDN Code
W02069003 CENTRIFUGES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

EUDAMEDEUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMEDEUDAMED

New Device

No

EUDAMED

Category: General-purpose centrifuge IVD

Rotofix 32 A by Andreas Hettich GmbH — 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
DE-MF-000010680

Sources (2)

  • EUDAMED 1620dd44-152e-4f7c-9c2b-1951beb37d93 61 fields · synced Jun 18, 2026
  • EUDAMED b2e05ef2-b803-4d90-8e29-3e23a2eb5e62 61 fields · synced Jun 18, 2026