eudamed_udi
Primary ID: 03664492021911
URGO Ongles Abîmés (UDI 03664492021911)
Manufactured by Laboratoires URGO HEALTHCARE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGO Ongles Abîmés - Primary ID 03664492021911
Device Regulatory Overview
The URGO Ongles Abîmés (Model/Catalog Number: 3664492021911) is a medical device manufactured by Laboratoires URGO HEALTHCARE. This product is indexed under FDA Product Code / Category Classification M0499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3664492021911
- Product Code / EMDN
- M0499
- Device Name
- URGO Damaged nails, filmogel
- Database Sync Date
- 2026-08-09 16:47:27
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 Ongles Abîmés?
The registered manufacturer of record for URGO Ongles Abîmés is Laboratoires URGO HEALTHCARE.
What is the Primary UDI-DI identifier for URGO Ongles Abîmés?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664492021911.
What classification code is assigned to this device?
This device is registered under product classification code M0499.
Similar Classification Devices (M0499)
Other Devices by Laboratoires URGO HEALTHCARE
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