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Relenza

EUDAMED

Class IIa (EU MDR)

Ref GLA28050A

by GlaxoSmithKline Trading Services Limited

Identity

Trade Name
Relenza EUDAMED
Device Name
Diskhaler EUDAMED
Model / Reference
GLA28050A EUDAMED

Identifiers

Primary DI / UDI-DI
85054363000444 EUDAMED
Basic UDI-DI
5054363591603257BA EUDAMED
Direct Marketing DI
85054363000444 EUDAMED
EMDN Code
R03010302 AEROSOL PORTABLE INHALERS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Relenza by GlaxoSmithKline Trading Services Limited — Class IIa — 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

EUDAMED SRN
IE-MF-000008351

Sources (1)

  • EUDAMED 6b19a675-16b4-4400-9e62-6cafb06588ff 61 fields · synced Jul 20, 2026