eudamed_udi
Primary ID: 03664492000749
URGO EXTENSIBLE (UDI 03664492000749)
Manufactured by Laboratoires URGO HEALTHCARE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGO EXTENSIBLE - Primary ID 03664492000749
Device Regulatory Overview
The URGO EXTENSIBLE (Model/Catalog Number: 3664492000749) is a medical device manufactured by Laboratoires URGO HEALTHCARE. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3664492000749
- Product Code / EMDN
- M04010101
- Device Name
- URGO EXTENSIBLE
- Database Sync Date
- 2026-08-09 16:47:12
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 URGO EXTENSIBLE?
The registered manufacturer of record for URGO EXTENSIBLE is Laboratoires URGO HEALTHCARE.
What is the Primary UDI-DI identifier for URGO EXTENSIBLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664492000749.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Laboratoires URGO HEALTHCARE
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