gudid
Primary ID: 509341
URGOTUL AG/SILVER (UDI 509341)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOTUL AG/SILVER - Primary ID 509341
Device Regulatory Overview
The URGOTUL AG/SILVER (Model/Catalog Number: 509341) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification FRO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 509341
- Product Code / EMDN
- FRO
- Device Name
- A non-adhesive and non-occlusive dressing consisting of a Silver Healing Matrix made of polyester mesh impregnated with hydrocolloid particles (carboxymethylcellulose), vaseline, cohesion polymers and Silver salts.
- Database Sync Date
- 2026-08-09 09:02:40
Full Regulatory Attributes
🔒 Token Gated
{
"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 URGOTUL AG/SILVER?
The registered manufacturer of record for URGOTUL AG/SILVER is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOTUL AG/SILVER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 509341.
What classification code is assigned to this device?
This device is registered under product classification code FRO.
Similar Classification Devices (FRO)
Other Devices by LABORATOIRES URGO
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