eudamed_udi
Primary ID: 03573026550448
ETEST® Cefixime (IX) (UDI 03573026550448)
Manufactured by bioMérieux SA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ETEST® Cefixime (IX) - Primary ID 03573026550448
Device Regulatory Overview
The ETEST® Cefixime (IX) (Model/Catalog Number: 8309001) is a medical device manufactured by bioMérieux SA. This product is indexed under FDA Product Code / Category Classification W0104080501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8309001
- Product Code / EMDN
- W0104080501
- Device Name
- ETEST® Cefixime (IX)
- Database Sync Date
- 2026-08-09 16:30:10
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 ETEST® Cefixime (IX)?
The registered manufacturer of record for ETEST® Cefixime (IX) is bioMérieux SA.
What is the Primary UDI-DI identifier for ETEST® Cefixime (IX)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03573026550448.
What classification code is assigned to this device?
This device is registered under product classification code W0104080501.
Similar Classification Devices (W0104080501)
Other Devices by bioMérieux SA
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