Identity
- Trade Name
- ARES EUDAMED
- Device Name
- Hemodialysis catheter kit EUDAMED
- Model / Reference
- ARES - HCT10003 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 86989077475730 EUDAMED
- Basic UDI-DI
- B-86989077475730 EUDAMED
- EMDN Code
- F900201 TEMPORARY HEMODIALYSIS CATHETERS AND KITS EUDAMED
Classification
- Device Class
- Class IIa 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 IIa — 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-86989077475730 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Ares Medikal Sanayi Ticaret Ltd. Şti.
- EUDAMED SRN
- TR-MF-000029015
Sources (1)
- EUDAMED e463a24d-d093-459c-a96c-b19e1f5aa360 61 fields · synced Oct 6, 2026