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Ares
EUDAMEDClass I (EU MDR)
Ref ARES - BID6000Model ARES - BID6000 - Balloon Inflation Device
Identity
- Trade Name
- ARES EUDAMED
- Device Name
- Balloon Inflation Device EUDAMED
- Model / Reference
- ARES - BID6000 - Balloon Inflation Device EUDAMEDARES - BID6000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 86989077410526 EUDAMED
- Basic UDI-DI
- B-86989077410526 EUDAMED
- EMDN Code
- C010401020180 PTCA BALLOON DILATATION CATHETERS - ACCESSORIES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Türkiye 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-86989077410526 | Class I | Active |
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Manufacturer
- Manufacturer
- Ares Medikal Sanayi Ticaret Ltd. Şti.
- EUDAMED SRN
- TR-MF-000029015
Sources (1)
- EUDAMED 7ced1d17-d3ce-4f82-8a06-8709ad5fc85c 61 fields · synced Oct 6, 2026