← Back to catalogue

Oxywise

EUDAMED

Class IIb (EU MDR)

Ref O9Model O1

by OXYWISE, s.r.o.

Identity

Trade Name
OXYWISE EUDAMED
Device Name
Medical Oxygen Generator EUDAMED
Model / Reference
O1 EUDAMED
O9 EUDAMED

Identifiers

Primary DI / UDI-DI
08588009198048 EUDAMED
Basic UDI-DI
085880091980MEDGENEB EUDAMED
Direct Marketing DI
08588009198048 EUDAMED
EMDN Code
R9099 RESPIRATORY AND ANAESTHESIA DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Slovakia 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

Category: Pulmonary function analysis system, adult

Oxywise by OXYWISE, s.r.o. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Pulmonary function analysis system, adult.

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
OXYWISE, s.r.o.
EUDAMED SRN
SK-MF-000034288

Sources (1)

  • EUDAMED 5ca40cfb-f4d2-43e2-b28d-7c426671d1df 61 fields · synced Jun 18, 2026