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Hematocrit Centrifuge

EUDAMED

Class A (EU MDR)

Ref iFuge HCT NXT

by Accumax Lab Devices Private Limited

Identity

Device Name: Hematocrit Centrifuge EUDAMED
Model / Reference: iFuge HCT NXT EUDAMED

Identifiers

Primary DI / UDI-DI: 89080197330064 EUDAMED
Basic UDI-DI: 8908019733ALDPL-CEN-001QX EUDAMED
Direct Marketing DI: 89080197330064 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

Hematocrit Centrifuge by Accumax Lab Devices Private Limited — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

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Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer: Accumax Lab Devices Private Limited
EUDAMED SRN: IN-MF-000028076
Authorised Representative: mdi Europa GmbH DE-AR-000006218

Sources (1)

EUDAMED f53c5b54-2d63-41af-81f4-37bd4d1f84d1 61 fields · synced Jun 19, 2026