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MAX 9k

EUDAMED

Class A (EU MDR)

Ref 17-0000-01

by MacroArray Diagnostics

Identity

Device Name
MAX 9k EUDAMED
Model / Reference
17-0000-01 EUDAMED

Identifiers

Primary DI / UDI-DI
09120122921708 EUDAMED
Basic UDI-DI
91201229217K5 EUDAMED
Direct Marketing DI
09120122921708 EUDAMED
EMDN Code
W0201020101 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Austria 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

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

MAX 9k by MacroArray Diagnostics — 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
AT-MF-000030541

Sources (1)

  • EUDAMED 80ba31b8-4067-482c-8964-7fd2c9e73e45 61 fields · synced Oct 5, 2026