Nelaton Catheter Female 8Ch (UDI 08682241350568)
Manufactured by TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ
Device Regulatory Overview
The Nelaton Catheter Female 8Ch (Model/Catalog Number: 104 0802 1) is a medical device manufactured by TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification U01010502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 104 0802 1
- Product Code / EMDN
- U01010502
- Device Name
- Nelaton Catheter
- Database Sync Date
- 2026-08-09 18:36:07
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 Nelaton Catheter Female 8Ch?
The registered manufacturer of record for Nelaton Catheter Female 8Ch is TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Nelaton Catheter Female 8Ch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682241350568.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ
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