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Mediflex
EUDAMEDClass IIa (EU MDR)
Ref FP 623-110/10Model Corrugated Circuit with Balloon and Water Trap
Identity
- Trade Name
- MEDIFLEX EUDAMED
- Device Name
- Anesthesia Breathing Circuit EUDAMED
- Model / Reference
- Corrugated Circuit with Balloon and Water Trap EUDAMEDFP 623-110/10 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08681277822162 EUDAMED
- Basic UDI-DI
- 868127782TD-C03HA EUDAMED
- Direct Marketing DI
- 08681277822162 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-C03HA | Class IIa | Active |
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Manufacturer
- Manufacturer
- Mediflex Medikal
- EUDAMED SRN
- TR-MF-000036464
Sources (1)
- EUDAMED d8c61e8b-87a5-4bdc-be7f-4c5bdde4bcba 61 fields · synced Jun 18, 2026