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Leishmania IgG/IgM Antibody Rapid Test
EUDAMEDClass IVD General (EU MDR)
Ref L-D22a
Identity
- Trade Name
- Leishmania IgG/IgM Antibody Rapid Test EUDAMED
- Device Name
- Leishmania IgG/IgM Antibody Rapid Test EUDAMED
- Model / Reference
- L-D22a EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-L-D22a43 EUDAMED
- Basic UDI-DI
- B-L-D22a43 EUDAMED
- EMDN Code
- W0105090499 PARASITES - RT & POC - OTHER EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
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
Leishmania IgG/IgM Antibody Rapid Test by Hangzhou Aichek Medical Technology Co., Ltd. — Class IVD General — IVDD — listed in EUDAMED
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-L-D22a43 | Class IVD General | Active |
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Manufacturer
- Manufacturer
- Hangzhou Aichek Medical Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000028093
- Authorised Representative
- Medunion S.L. ES-AR-000019366
Sources (1)
- EUDAMED d7664bcc-41dc-4749-803c-434f710e4550 61 fields · synced Jun 18, 2026