eudamed_udi
Primary ID: 86989077477406
ARES (UDI 86989077477406)
Manufactured by Ares Medikal Sanayi Ticaret Ltd. Şti.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ARES - Primary ID 86989077477406
Device Regulatory Overview
The ARES (Model/Catalog Number: ARES - HCT10020) is a medical device manufactured by Ares Medikal Sanayi Ticaret Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification F900201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ARES - HCT10020
- Product Code / EMDN
- F900201
- Device Name
- Hemodialysis catheter kit
- Database Sync Date
- 2026-08-09 16:49:22
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of ARES?
The registered manufacturer of record for ARES is Ares Medikal Sanayi Ticaret Ltd. Şti..
What is the Primary UDI-DI identifier for ARES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 86989077477406.
What classification code is assigned to this device?
This device is registered under product classification code F900201.
Similar Classification Devices (F900201)
Other Devices by Ares Medikal Sanayi Ticaret Ltd. Şti.
Programmatic Export
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