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LiCA Toxo lgG

EUDAMED

Class C (EU MDR)

Ref 05010828322Model 2 × 50 Tests; 2 × 50 Tests; 2 × 100 Tests; 4 × 100 Tests

by Chemclin Diagnostics Co., Ltd.

Identity

Trade Name
LiCA Toxo lgG EUDAMED
Device Name
LiCA Toxo IgG EUDAMED
Model / Reference
2 × 50 Tests; 2 × 50 Tests; 2 × 100 Tests; 4 × 100 Tests EUDAMED
05010828322 EUDAMED

Identifiers

Primary DI / UDI-DI
06973864382657 EUDAMED
Basic UDI-DI
6973864380046EU EUDAMED
EMDN Code
W0105050102 TOXOPLASMA ANTIBODY IGG EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

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

LiCA Toxo lgG by Chemclin Diagnostics Co., Ltd. — Class C — 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
CN-MF-000009729
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 62929a0b-a32c-4d92-8eb5-a1c6ad141f50 61 fields · synced Jul 11, 2026