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Mediflex
EUDAMEDClass IIa (EU MDR)
Ref MFA 623-209 /300400700800Model With Balloon, Water Trap, and Catheter
Identity
- Trade Name
- MEDIFLEX EUDAMED
- Device Name
- Anesthesia Breathing Circuit EUDAMED
- Model / Reference
- With Balloon, Water Trap, and Catheter EUDAMEDMFA 623-209 /300400700800 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08681277822025 EUDAMED
- Basic UDI-DI
- 868127782TD-013EK EUDAMED
- Direct Marketing DI
- 08681277822025 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
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 868127782TD-013EK | Class IIa | Active |
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Manufacturer
- Manufacturer
- Mediflex Medikal
- EUDAMED SRN
- TR-MF-000036464
Sources (1)
- EUDAMED 5cce7678-84e7-43f4-9358-22b358332916 61 fields · synced Jun 18, 2026