Identity
- Trade Name
- ARES EUDAMED
- Device Name
- Balloon Inflation Device EUDAMED
- Model / Reference
- BID6000 EUDAMEDSBID3520KSTT EUDAMED
Identifiers
- Primary DI / UDI-DI
- 86989077504294 EUDAMED
- Basic UDI-DI
- B-86989077504294 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
Category: Peripheral angioplasty balloon catheter, basic
Ares by Ares Medikal Sanayi Ticaret Ltd. Şti. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Similar devices
Also classified as Peripheral angioplasty balloon catheter, basic.
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- Armada — Abbott Vascular · Class II
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-86989077504294 | Class I | Active |
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Manufacturer
- Manufacturer
- Ares Medikal Sanayi Ticaret Ltd. Şti.
- EUDAMED SRN
- TR-MF-000029015
Sources (1)
- EUDAMED ada4c5a4-f335-4047-ae69-da46a7fdf7a9 61 fields · synced Jun 20, 2026