Identity
- Device Name
- NASAL AIRWAY 28FR EUDAMED
- Model / Reference
- PDF228 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 50604835729010 EUDAMED
- Basic UDI-DI
- 506048357PDF2283K EUDAMED
- EMDN Code
- R010202 LARYNGEAL TUBES EUDAMED
Classification
- Device Class
- Class I 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
Nasal Airway 28fr by Safeguard Medical Technologies — 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 | 506048357PDF2283K | Class I | Active |
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Manufacturer
- Manufacturer
- Safeguard Medical Technologies Ltd.
- EUDAMED SRN
- GB-MF-000012038
- Authorised Representative
- Safeguard Medical Nordic AB SE-AR-000048667
Sources (1)
- EUDAMED d0cec039-2791-4955-8801-2de25f3815bf 61 fields · synced Aug 2, 2026