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Mediflex

EUDAMED

Class IIa (EU MDR)

Ref F 501Model CPAP

by Mediflex Medikal

Identity

Trade Name
MEDIFLEX EUDAMED
Device Name
Ventilator Breathing Circuit EUDAMED
Model / Reference
CPAP EUDAMED
F 501 EUDAMED

Identifiers

Primary DI / UDI-DI
08681277821066 EUDAMED
Basic UDI-DI
868127782TD-015EP EUDAMED
Direct Marketing DI
08681277821066 EUDAMED
EMDN Code
R02010401 CPAP CIRCUITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Türkiye 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

Mediflex by Mediflex Medikal — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Mediflex Medikal
EUDAMED SRN
TR-MF-000036464

Sources (1)

  • EUDAMED b4ed9699-6650-46fc-93db-7e94822ec959 61 fields · synced Jun 18, 2026