Identity
- Trade Name
- Test Lung 1000 ml EUDAMED
- Device Name
- Test Lung EUDAMED
- Model / Reference
- MY151022 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07350045121691 EUDAMED
- Basic UDI-DI
- 73500451241531313ZB EUDAMED
- EMDN Code
- R020199 BREATHING CIRCUITS AND KITS - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Sweden EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Test Lung 1000 ml by Kanmed AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 73500451241531313ZB | Class I | Active |
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Manufacturer
- Manufacturer
- Kanmed AB
- EUDAMED SRN
- SE-MF-000001839
Sources (1)
- EUDAMED 05ca4488-a708-4b61-a6e9-946799ec3f2b 61 fields · synced Jun 19, 2026