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Nasaleze Allergy Blocker

EUDAMED

Class I (EU MDR)

Ref NAB01Model HPMC+Peppermint Powder

by Nasaleze Limited

Identity

Trade Name
Nasaleze Allergy Blocker EUDAMED
Device Name
Nasaleze Allergy Blocker EUDAMED
Model / Reference
HPMC+Peppermint Powder EUDAMED
NAB01 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

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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