eudamed_udi
Primary ID: 03546890045709
URGOSTART Border (UDI 03546890045709)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOSTART Border - Primary ID 03546890045709
Device Regulatory Overview
The URGOSTART Border (Model/Catalog Number: 603719) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification M04040602 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 603719
- Product Code / EMDN
- M04040602
- Device Name
- URGOSTART Border
- Database Sync Date
- 2026-08-09 16:46:55
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 URGOSTART Border?
The registered manufacturer of record for URGOSTART Border is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOSTART Border?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03546890045709.
What classification code is assigned to this device?
This device is registered under product classification code M04040602.
Similar Classification Devices (M04040602)
Other Devices by LABORATOIRES URGO
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint