GoldCath (UDI 08680110403551)
Manufactured by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ
Device Regulatory Overview
The GoldCath (Model/Catalog Number: 2006) is a medical device manufactured by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET 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
- 2006
- Product Code / EMDN
- U01010502
- Device Name
- Urinary Nelaton Catheter
- Database Sync Date
- 2026-08-09 16:46:17
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 GoldCath?
The registered manufacturer of record for GoldCath is DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ.
What is the Primary UDI-DI identifier for GoldCath?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08680110403551.
What classification code is assigned to this device?
This device is registered under product classification code U01010502.
Similar Classification Devices (U01010502)
Other Devices by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ
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