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Cuvettes Rack Pentra C200

EUDAMED

Class A (EU MDR)

Ref A11A01914

by Horiba Abx Sas

Identity

Trade Name
CUVETTES RACK PENTRA C200 EUDAMED
Device Name
CUVETTES RACK PENTRA C200 EUDAMED
Model / Reference
A11A01914 EUDAMED

Identifiers

Primary DI / UDI-DI
03610230005644 EUDAMED
Basic UDI-DI
361023cuvette_rackPM EUDAMED
EMDN Code
W0503010203 SAMPLES ANALYSES, PLASTIC CUVETTES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France 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

No

EUDAMED

New Device

No

EUDAMED

Cuvettes Rack Pentra C200 by Horiba Abx Sas — 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

Manufacturer
Horiba Abx Sas
EUDAMED SRN
FR-MF-000000320

Sources (1)

  • EUDAMED 3d02a478-7000-4e2c-9090-5b7e97d6869f 61 fields · synced Aug 4, 2026