Identity
- Trade Name
- ARES EUDAMED
- Device Name
- Balloon Inflation Device EUDAMED
- Model / Reference
- BID6000 EUDAMEDSBID3020KPPT EUDAMED
Identifiers
- Primary DI / UDI-DI
- 86989077502450 EUDAMED
- Basic UDI-DI
- B-86989077502450 EUDAMED
- EMDN Code
- C010402020101 PTA BALLOON DILATATION CATHETERS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Italy EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Ares by Ares Medikal Sanayi Ticaret Ltd. Şti. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-86989077502450 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Ares Medikal Sanayi Ticaret Ltd. Şti.
- EUDAMED SRN
- TR-MF-000029015
Sources (1)
- EUDAMED b8a36ef7-d035-41ec-bf60-fbd1c51fccae 61 fields · synced Oct 6, 2026