← Back to catalogue

Otovent

EUDAMED

Class I (EU MDR)

Ref 50102

by Circius Pharma AB

Identity

Trade Name
Otovent EUDAMED
Device Name
Otovent EUDAMED
Model / Reference
50102 EUDAMED

Identifiers

Primary DI / UDI-DI
07350133960201 EUDAMED
Basic UDI-DI
735013396Otovent1TV EUDAMED
EMDN Code
Q03040199 EAR DRAINAGE AND VENTILATION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Otovent by Circius Pharma AB — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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

Manufacturer

Manufacturer
Circius Pharma AB
EUDAMED SRN
SE-MF-000013023

Sources (1)

  • EUDAMED 351a3f14-b426-4423-84ed-eda497372d72 61 fields · synced Jun 18, 2026