eudamed_udi
Primary ID: 03573026240400
VIDAS® FT4 (UDI 03573026240400)
Manufactured by bioMérieux SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VIDAS® FT4 - Primary ID 03573026240400
Device Regulatory Overview
The VIDAS® FT4 (Model/Catalog Number: 30459) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W01020402 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30459
- Product Code / EMDN
- W01020402
- Device Name
- VIDAS® FT4
- Database Sync Date
- 2026-08-09 16:50:24
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® FT4?
The registered manufacturer of record for VIDAS® FT4 is bioMérieux SA.
What is the Primary UDI-DI identifier for VIDAS® FT4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026240400.
What classification code is assigned to this device?
This device is registered under product classification code W01020402.
Similar Classification Devices (W01020402)
Other Devices by bioMérieux SA
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