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Mediflex

EUDAMED

Class IIa (EU MDR)

Ref FA 623-209/300400700800 Model Corrugated Circuit with Balloon, Water Trap and Catheter

by Mediflex Medikal

Identity

Trade Name
MEDIFLEX EUDAMED
Device Name
Anesthesia Breathing Circuit EUDAMED
Model / Reference
Corrugated Circuit with Balloon, Water Trap and Catheter EUDAMED
FA 623-209/300400700800 EUDAMED

Identifiers

Primary DI / UDI-DI
08681277822193 EUDAMED
Basic UDI-DI
868127782TD-C04HC EUDAMED
Direct Marketing DI
08681277822193 EUDAMED
EMDN Code
R028099 RESPIRATORY CIRCUITS AND MOUNT CATHETERS - ACCESSORIES NOT INCLUDED IN OTHER CLASSES 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 8c688045-5d9f-4b84-8415-06c4f5c5cbfe 61 fields · synced Jun 19, 2026