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ROTOFIX 32 A, 100-127V 50-60Hz, (MD)

EUDAMED

Class IIa (EU MDR)

Ref 1207-01Model 1207

by Andreas Hettich GmbH

Identity

Trade Name
ROTOFIX 32 A, 100-127V 50-60Hz, (MD) EUDAMED
Device Name
ROTOFIX 32 A (MD) EUDAMED
Model / Reference
1207 EUDAMED
1207-01 EUDAMED

Identifiers

Primary DI / UDI-DI
04050674098120 EUDAMED
Basic UDI-DI
040506740100259Y EUDAMED
Direct Marketing DI
04050674098120 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, 100-127V 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 12cbe053-807a-44df-8662-d9ea014311d7 61 fields · synced Jul 13, 2026
  • EUDAMED cd356999-9bc0-46c9-a4c3-4463ddf4643f 61 fields · synced Jul 13, 2026