← Back to catalogue

Revolizer

EUDAMED

Class I (EU MDR)

Ref Not Applicable for Revolizer

by Cipla Limited

Identity

Device Name
Revolizer EUDAMED
Model / Reference
Not Applicable for Revolizer EUDAMED

Identifiers

Primary DI / UDI-DI
D-8901117REV0123QLWV EUDAMED
Basic UDI-DI
B-8901117REV0123QLWV EUDAMED
EMDN Code
R900901 INHALERS EUDAMED

Classification

Device Class
Class I 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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Revolizer by Cipla Limited — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union No Longer Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Cipla Limited
EUDAMED SRN
IN-MF-000038939
Authorised Representative
Cipla Europe NV BE-AR-000038918

Sources (1)

  • EUDAMED 1e9d9a43-fb37-49b0-8e3b-62f2fa210795 61 fields · synced Jun 19, 2026