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Patient Interfaces（Nasal Cannula）
EUDAMEDClass IIa (EU MDR)
Ref NAModel Hi-NAI-L, Hi-NAI-M, Hi-NAI-S
Identity
- Device Name
- Patient Interfaces（Nasal Cannula） EUDAMED
- Model / Reference
- Hi-NAI-L, Hi-NAI-M, Hi-NAI-S EUDAMEDNA EUDAMED
Identifiers
- Primary DI / UDI-DI
- 16975984064540 EUDAMED
- Basic UDI-DI
- 6970341680112301GY EUDAMED
- Direct Marketing DI
- 16975984064540 EUDAMED
- EMDN Code
- R060280 HUMIDIFICATION SYSTEMS - ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Ireland 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
Patient Interfaces（Nasal Cannula） by Shenzhen Lifotronic Technology Co., Ltd. — Class IIa — 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 | 6970341680112301GY | Class IIa | Active |
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Manufacturer
- Manufacturer
- Shenzhen Lifotronic Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000005654
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (2)
- EUDAMED ae53daa1-f9ba-4349-b9fe-43ba1e77fab3 61 fields · synced Sep 18, 2026
- EUDAMED ae53daa1-f9ba-4349-b9fe-43ba1e77fab3-1 61 fields · synced Jun 10, 2026