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ROTOFIX 32 A, 208-240V 50-60Hz, (MD)

EUDAMED

Class IIa (EU MDR)

Ref 1207

by Andreas Hettich GmbH

Identity

Trade Name
ROTOFIX 32 A, 208-240V 50-60Hz, (MD) EUDAMED
Device Name
ROTOFIX 32 A (MD) EUDAMED
Model / Reference
1207 EUDAMED

Identifiers

Primary DI / UDI-DI
04050674098113 EUDAMED
Basic UDI-DI
040506740100259Y EUDAMED
Direct Marketing DI
04050674098113 EUDAMED
EMDN Code
W02069003 CENTRIFUGES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: General-purpose centrifuge IVD

ROTOFIX 32 A, 208-240V 50-60Hz, (MD) by Andreas Hettich GmbH — Class IIa — MDR — 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/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000010680

Sources (2)

  • EUDAMED 8605683a-a062-448c-a4f4-ea52c9dc2d71 61 fields · synced Jun 19, 2026
  • EUDAMED c5120171-78eb-443f-8ba8-8e4735526389 61 fields · synced Jun 19, 2026