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Nasaleze Travel
EUDAMEDClass I (EU MDR)
Ref NT01Model HPMC+European Wild Garlic+ Peppermint Powder
Identity
- Trade Name
- Nasaleze Travel EUDAMED
- Device Name
- Nasaleze Travel EUDAMED
- Model / Reference
- HPMC+European Wild Garlic+ Peppermint Powder EUDAMEDNT01 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060045000118 EUDAMED
- Basic UDI-DI
- 5060045NT01TL EUDAMED
- Direct Marketing DI
- 05060045000118 EUDAMED
- EMDN Code
- M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) EUDAMED
Classification
- Device Class
- Class I 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
Nasaleze Travel by Nasaleze Limited — 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 | 5060045NT01TL | Class I | Active |
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Manufacturer
- Manufacturer
- Nasaleze Limited
- EUDAMED SRN
- IM-MF-000004004
- Authorised Representative
- Acorn Regulatory Consultancy Services Ltd IE-AR-000000592
Sources (1)
- EUDAMED fade87a6-0280-4bf4-bb0d-7340d4a9f03a 61 fields · synced Jun 19, 2026