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Viraleze™

EUDAMED

Class I (EU MDR)

Ref PM53.3.0EUModel N001

by Starpharma Pty Ltd

Identity

Trade Name
VIRALEZE™ EUDAMED
Device Name
VIRALEZE™ Nasal Spray EUDAMED
Model / Reference
N001 EUDAMED
PM53.3.0EU EUDAMED

Identifiers

Primary DI / UDI-DI
09354505000333 EUDAMED
Basic UDI-DI
B-09354505000333 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
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Viraleze™ by Starpharma Pty Ltd — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Starpharma Pty Ltd
EUDAMED SRN
AU-MF-000012162
Authorised Representative
Qualrep Services B.V. NL-AR-000000537

Sources (1)

  • EUDAMED 8c6e249c-7903-498d-a0cc-95146dc3219e 61 fields · synced Jul 13, 2026