eudamed_udi
Primary ID: 03546890032112
URGOSTART Plus Kompresse (UDI 03546890032112)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGOSTART Plus Kompresse - Primary ID 03546890032112
Device Regulatory Overview
The URGOSTART Plus Kompresse (Model/Catalog Number: 754187) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification M040499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 754187
- Product Code / EMDN
- M040499
- Device Name
- URGOSTART PLUS Pad - URGOSTART PLUS Compresse - URGOSTART PLUS Kompresse
- Database Sync Date
- 2026-08-09 16:30:37
Full Regulatory Attributes
π Token Gated
{
"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 URGOSTART Plus Kompresse?
The registered manufacturer of record for URGOSTART Plus Kompresse is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGOSTART Plus Kompresse?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03546890032112.
What classification code is assigned to this device?
This device is registered under product classification code M040499.
Similar Classification Devices (M040499)
Other Devices by LABORATOIRES URGO
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