eudamed_udi
Primary ID: 03546890047529
URGO K2 (UDI 03546890047529)
Manufactured by LABORATOIRES URGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for URGO K2 - Primary ID 03546890047529
Device Regulatory Overview
The URGO K2 (Model/Catalog Number: 604221) is a medical device manufactured by LABORATOIRES URGO. This product is indexed under FDA Product Code / Category Classification M03040199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 604221
- Product Code / EMDN
- M03040199
- Device Name
- URGO K2 - URGO KTwo
- Database Sync Date
- 2026-08-09 16:29:48
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 K2?
The registered manufacturer of record for URGO K2 is LABORATOIRES URGO.
What is the Primary UDI-DI identifier for URGO K2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03546890047529.
What classification code is assigned to this device?
This device is registered under product classification code M03040199.
Similar Classification Devices (M03040199)
Other Devices by LABORATOIRES URGO
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