GUDIDData
eudamed_udi Primary ID: 08680110400758

GoldCath (UDI 08680110400758)

Manufactured by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GoldCath - Primary ID 08680110400758

Device Regulatory Overview

The GoldCath (Model/Catalog Number: 4006) is a medical device manufactured by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ. This product is indexed under FDA Product Code / Category Classification U01010501 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
4006
Product Code / EMDN
U01010501
Device Name
Hydrophilic Urinary Kit
Database Sync Date
2026-08-09 16:28:47

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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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 08680110400758.

What classification code is assigned to this device?

This device is registered under product classification code U01010501.

Similar Classification Devices (U01010501)

Other Devices by DEMERSAN BIYOTEKNOLOJI İMALAT SANAYİ VE TİCARET ANONİM ŞİRKETİ

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