Nelaton Catheter Female 12Ch (UDI 08682241350582)
Manufactured by TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ
Device Regulatory Overview
The Nelaton Catheter Female 12Ch (Model/Catalog Number: 104 1202 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 1202 1
- Product Code / EMDN
- U01010502
- Device Name
- Nelaton Catheter
- Database Sync Date
- 2026-08-09 16:48:15
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Nelaton Catheter Female 12Ch?
The registered manufacturer of record for Nelaton Catheter Female 12Ch is TÜREV İÇ VE DIŞ TİC. ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for Nelaton Catheter Female 12Ch?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08682241350582.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint