eudamed_udi
Primary ID: 03664492025414
URGOPORE (UDI 03664492025414)
Manufactured by Laboratoires URGO HEALTHCARE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOPORE - Primary ID 03664492025414
Device Regulatory Overview
The URGOPORE (Model/Catalog Number: 3664492025414) is a medical device manufactured by Laboratoires URGO HEALTHCARE. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3664492025414
- Product Code / EMDN
- M050101
- Device Name
- URGOPORE
- Database Sync Date
- 2026-08-09 17:02:53
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 URGOPORE?
The registered manufacturer of record for URGOPORE is Laboratoires URGO HEALTHCARE.
What is the Primary UDI-DI identifier for URGOPORE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664492025414.
What classification code is assigned to this device?
This device is registered under product classification code M050101.
Similar Classification Devices (M050101)
Other Devices by Laboratoires URGO HEALTHCARE
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