eudamed_udi
Primary ID: 03546890050819
URGO K1 (UDI 03546890050819)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGO K1 - Primary ID 03546890050819
Device Regulatory Overview
The URGO K1 (Model/Catalog Number: 605800) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification M0304010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 605800
- Product Code / EMDN
- M0304010102
- Device Name
- URGO K1 - URGO KOne
- Database Sync Date
- 2026-08-09 16:45:51
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 K1?
The registered manufacturer of record for URGO K1 is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGO K1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03546890050819.
What classification code is assigned to this device?
This device is registered under product classification code M0304010102.
Similar Classification Devices (M0304010102)
Other Devices by LABORATOIRES URGO
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