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Nasaleze Allergy Blocker
EUDAMEDClass I (EU MDR)
Ref NAB01Model HPMC+Peppermint Powder
Identity
- Trade Name
- Nasaleze Allergy Blocker EUDAMED
- Device Name
- Nasaleze Allergy Blocker EUDAMED
- Model / Reference
- HPMC+Peppermint Powder EUDAMEDNAB01 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060045001337 EUDAMED
- Basic UDI-DI
- 5060045NAB01HW EUDAMED
- Direct Marketing DI
- 05060045001337 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 Allergy Blocker 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 | 5060045NAB01HW | 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 96a4b8eb-e7d2-46fe-838b-60c8d8595075 61 fields · synced Jul 9, 2026