eudamed_udi
Primary ID: 03573026073824
Urée-Arginine LYO 2 (UDI 03573026073824)
Manufactured by bioMérieux SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Urée-Arginine LYO 2 - Primary ID 03573026073824
Device Regulatory Overview
The Urée-Arginine LYO 2 (Model/Catalog Number: 42508) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W0104080207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 42508
- Product Code / EMDN
- W0104080207
- Device Name
- Urée-Arginine LYO 2
- Database Sync Date
- 2026-08-09 17:48:20
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 Urée-Arginine LYO 2?
The registered manufacturer of record for Urée-Arginine LYO 2 is bioMérieux SA.
What is the Primary UDI-DI identifier for Urée-Arginine LYO 2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026073824.
What classification code is assigned to this device?
This device is registered under product classification code W0104080207.
Similar Classification Devices (W0104080207)
Other Devices by bioMérieux SA
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