gudid
Primary ID: 604230
URGOTUL (UDI 604230)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOTUL - Primary ID 604230
Device Regulatory Overview
The URGOTUL (Model/Catalog Number: 604230) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification NAC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 604230
- Product Code / EMDN
- NAC
- Device Name
- A non-occlusive flexible and conformable dressing comprising of a polyester mesh impregnated with hydrocolloid particle dispersed in a petroleum jelly matrix.
- Database Sync Date
- 2026-08-09 09:46:57
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 URGOTUL?
The registered manufacturer of record for URGOTUL is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOTUL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 604230.
What classification code is assigned to this device?
This device is registered under product classification code NAC.
Similar Classification Devices (NAC)
Other Devices by LABORATOIRES URGO
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