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Optiflow

EUDAMED

Class IIa (EU MDR)

Ref 63.00.272

by Ardo medical AG

Identity

Trade Name
OPTIFLOW EUDAMED
Device Name
OPTIFLOW EUDAMED
Model / Reference
63.00.272 EUDAMED

Identifiers

Primary DI / UDI-DI
07640109053922 EUDAMED
Basic UDI-DI
B-07640109053922 EUDAMED
EMDN Code
V020302 BABY BOTTLES AND KIT EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany 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

Optiflow by Ardo medical AG — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Ardo medical AG
EUDAMED SRN
CH-MF-000016526
Authorised Representative
ARDO medical GmbH DE-AR-000014440

Sources (1)

  • EUDAMED bdcd1a31-3ff8-4f84-bf6a-aa9db34fbf67 61 fields · synced Oct 6, 2026