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iFuge CS2P NXT

EUDAMED

Class A (EU MDR)

Ref iFuge CS2P NXTModel iFuge CS2P

by Accumax Lab Devices Private Limited

Identity

Trade Name
iFuge CS2P NXT EUDAMED
Device Name
Micro Plate Centrifuge EUDAMED
Model / Reference
iFuge CS2P EUDAMED
iFuge CS2P NXT EUDAMED

Identifiers

Primary DI / UDI-DI
89080197336868 EUDAMED
Basic UDI-DI
8908019733CLI-CEN-04TP EUDAMED
Direct Marketing DI
89080197336868 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

iFuge CS2P NXT by Accumax Lab Devices Private Limited — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

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 f5d7cbe8-536e-43e2-bf8b-f9f5a90f5606 61 fields · synced Jun 17, 2026