eudamed_udi
Primary ID: 03664492017495
URGOFILM (UDI 03664492017495)
Manufactured by Laboratoires URGO HEALTHCARE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOFILM - Primary ID 03664492017495
Device Regulatory Overview
The URGOFILM (Model/Catalog Number: 3664492017495) is a medical device manufactured by Laboratoires URGO HEALTHCARE. This product is indexed under FDA Product Code / Category Classification H900299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3664492017495
- Product Code / EMDN
- H900299
- Device Name
- URGOPLASTIC FILM TRANSPARENT
- Database Sync Date
- 2026-08-09 16:30:20
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 URGOFILM?
The registered manufacturer of record for URGOFILM is Laboratoires URGO HEALTHCARE.
What is the Primary UDI-DI identifier for URGOFILM?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664492017495.
What classification code is assigned to this device?
This device is registered under product classification code H900299.
Similar Classification Devices (H900299)
Other Devices by Laboratoires URGO HEALTHCARE
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