gudid
Primary ID: 553245
URGOK2 LITE (UDI 553245)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOK2 LITE - Primary ID 553245
Device Regulatory Overview
The URGOK2 LITE (Model/Catalog Number: 553245) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 553245
- Product Code / EMDN
- FQM
- Device Name
- A 2-layer reduced multicomponent compression bandage system, composed of a short stretch bandage and a long stretch bandage.Layer 1, KTECH Lite/KTECH Reduced composition: wadding: viscose, polyester; knitted layer: polyamide, elastane.Layer 2, KPRESS composition: cotton, polyester, polyamide, elastane; synthetic latex free cohesive material.
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of URGOK2 LITE?
The registered manufacturer of record for URGOK2 LITE is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOK2 LITE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 553245.
What classification code is assigned to this device?
This device is registered under product classification code FQM.
Similar Classification Devices (FQM)
Other Devices by LABORATOIRES URGO
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint