eudamed_udi
Primary ID: 03573026265076
VIDAS® Lyme IgG (UDI 03573026265076)
Manufactured by bioMérieux SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIDAS® Lyme IgG - Primary ID 03573026265076
Device Regulatory Overview
The VIDAS® Lyme IgG (Model/Catalog Number: 30320) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W0105010603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30320
- Product Code / EMDN
- W0105010603
- Device Name
- VIDAS® Lyme IgG
- Database Sync Date
- 2026-08-09 16:50:59
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 VIDAS® Lyme IgG?
The registered manufacturer of record for VIDAS® Lyme IgG is bioMérieux SA.
What is the Primary UDI-DI identifier for VIDAS® Lyme IgG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026265076.
What classification code is assigned to this device?
This device is registered under product classification code W0105010603.
Similar Classification Devices (W0105010603)
Other Devices by bioMérieux SA
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