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Oxywise

EUDAMED

Class IIb (EU MDR)

Ref O50+

by OXYWISE, s.r.o.

Identity

Trade Name
OXYWISE EUDAMED
Device Name
Medical Oxygen Generator EUDAMED
Model / Reference
O50+ EUDAMED

Identifiers

Primary DI / UDI-DI
08588009198147 EUDAMED
Basic UDI-DI
B-08588009198147 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

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

Category: Pulmonary function analysis system, adult

Oxywise by OXYWISE, s.r.o. — Class IIb — MDD — 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/MDD

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Manufacturer

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

Sources (1)

  • EUDAMED 56bf0ad6-91b7-4731-8cc1-ba8e8b446729 61 fields · synced Jul 21, 2026