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TTÅniKoReader®

EUDAMED

Class A (EU MDR)

Ref KM102

by KH Medical Co., Ltd.

Identity

Trade Name
TTÅniKoReader® EUDAMED
Device Name
TTÅniKoReader EUDAMED
Model / Reference
KM102 EUDAMED

Identifiers

Primary DI / UDI-DI
08800204301826 EUDAMED
Basic UDI-DI
880002043ImmunoequipFH EUDAMED
EMDN Code
W02050199 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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

TTÅniKoReader® by KH Medical 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

EUDAMED SRN
KR-MF-000017883
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED ae70f2f5-1c86-4922-ac22-b8725aeb627f 61 fields · synced Jul 14, 2026