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Rotolavit Ii

EUDAMED

Class A (EU MDR)

Ref 1008-00

by Hettich AG

Identity

Trade Name
ROTOLAVIT II EUDAMED
Device Name
ROTOLAVIT II, 100-240V, 50-60HZ, OHNE ROTOR EUDAMED
Model / Reference
1008-00 EUDAMED

Identifiers

Primary DI / UDI-DI
07640173551003 EUDAMED
Basic UDI-DI
07640173551008-0029 EUDAMED
Direct Marketing DI
07640173551003 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

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: General-purpose centrifuge IVD

Rotolavit Ii by Hettich AG — 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

Manufacturer
Hettich AG
EUDAMED SRN
CH-MF-000041657
Authorised Representative
Andreas Hettich GmbH DE-AR-000016247

Sources (1)

  • EUDAMED 28c2a5b7-c6f8-4fb2-b10b-a3bfe9f0a163 61 fields · synced Jul 8, 2026