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Mediflex
EUDAMEDClass IIa (EU MDR)
Ref MFA 623-209/20 Model With Balloon and 2 Water Trap
Identity
- Trade Name
- MEDIFLEX EUDAMED
- Device Name
- Anesthesia Breathing Circuit EUDAMED
- Model / Reference
- With Balloon and 2 Water Trap EUDAMEDMFA 623-209/20 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08681277822070 EUDAMED
- Basic UDI-DI
- 868127782TD-014EM EUDAMED
- Direct Marketing DI
- 08681277822070 EUDAMED
- EMDN Code
- R02010102 BREATHING CIRCUITS, WITH WATER TRAP 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-014EM | Class IIa | Active |
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Manufacturer
- Manufacturer
- Mediflex Medikal
- EUDAMED SRN
- TR-MF-000036464
Sources (1)
- EUDAMED b8637ba3-d81b-4be9-bd87-b10dcb76026b 61 fields · synced Jun 18, 2026