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iFuge CYTO

EUDAMED

Class A (EU MDR)

Ref iFuge CYTO

by Accumax Lab Devices Private Limited

Identity

Trade Name
iFuge CYTO EUDAMED
Device Name
Cytoslide Centrifuge iFuge CYTO EUDAMED
Model / Reference
iFuge CYTO EUDAMED

Identifiers

Primary DI / UDI-DI
89080197336622 EUDAMED
Basic UDI-DI
8908019733CLI-CEN-06TT EUDAMED
Direct Marketing DI
89080197336622 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

iFuge CYTO by Accumax Lab Devices Private Limited — 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
IN-MF-000028076
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (1)

  • EUDAMED 4d5c9f83-26c6-4f05-8f8f-91125fdd344d 61 fields · synced Jul 13, 2026