gudid
Primary ID: 509346
URGOCELL AG/SILVER (UDI 509346)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOCELL AG/SILVER - Primary ID 509346
Device Regulatory Overview
The URGOCELL AG/SILVER (Model/Catalog Number: 509346) 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
- 509346
- Product Code / EMDN
- FRO
- Device Name
- A non-occlusive semi-permeable absorbent dressing impregnated with Silver Salts derived from Technology Lipido-Colloid (TLC). Composed of 3 layers :- Silver Healing Matrix TLC-Ag made of polyester mesh impregnated with hydrocolloid particles (carboxymethylcellulose), vaseline, cohesion polymers and Silver salts- an absorbent polyurethane foam pad- a protective polyurethane backing
- Database Sync Date
- 2026-08-09 09:02:40
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 URGOCELL AG/SILVER?
The registered manufacturer of record for URGOCELL AG/SILVER is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOCELL AG/SILVER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 509346.
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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