Identity
- Device Name
- Nuflow EUDAMED
- Model / Reference
- 1340 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04060139400139 EUDAMED
- Basic UDI-DI
- 4060139000072P EUDAMED
- EMDN Code
- R0301020302 HIGH FLOW THERAPY NASAL CANNULAS (HFNC) EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany 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
Nuflow by medin Medical Innovations GmbH — 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 | 4060139000072P | Class IIa | Active |
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Manufacturer
- Manufacturer
- medin Medical Innovations GmbH
- EUDAMED SRN
- DE-MF-000006975
Sources (1)
- EUDAMED 765725d9-1f87-46b6-ac4e-1a5fef99ab23 61 fields · synced Oct 6, 2026