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Coagulation Analyzer

EUDAMED

Class A (EU MDR)

Ref IN0126Model BCA Series, CA Series

by Infitek Co., Ltd.

Identity

Trade Name
Coagulation Analyzer EUDAMED
Device Name
Coagulation Analyzer EUDAMED
Model / Reference
BCA Series, CA Series EUDAMED
IN0126 EUDAMED

Identifiers

Primary DI / UDI-DI
06978507780241 EUDAMED
Basic UDI-DI
697850778BCA10L5 EUDAMED
EMDN Code
W0103020199 GENERAL COAGULATION TESTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Türkiye 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

Coagulation Analyzer by Infitek Co., Ltd. — 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
Infitek Co., Ltd.
EUDAMED SRN
CN-MF-000048840
Authorised Representative
Kingsmead Service B.V. NL-AR-000002066

Sources (1)

  • EUDAMED 770fb537-6155-4be1-92f8-db0c483648c0 61 fields · synced Jun 19, 2026