gudid
Primary ID: BACT/ALERT FA
BACT/ALERT FA (UDI BACT/ALERT FA)
Manufactured by BIOMERIEUX , INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BACT/ALERT FA - Primary ID BACT/ALERT FA
Device Regulatory Overview
The BACT/ALERT FA (Model/Catalog Number: BACT/ALERT FA) is a medical device manufactured by BIOMERIEUX , INC.. This product is indexed under FDA Product Code / Category Classification MDB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BACT/ALERT FA
- Product Code / EMDN
- MDB
- Device Name
- The BACT/ALERT FA Culture Bottles are used for enhanced recovery and detection of aerobic and facultative anaerobic microorganisms from blood, other normally sterile body fluids.
- Database Sync Date
- 2026-08-09 09:46:56
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 BACT/ALERT FA?
The registered manufacturer of record for BACT/ALERT FA is BIOMERIEUX , INC..
What is the Primary UDI-DI identifier for BACT/ALERT FA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BACT/ALERT FA.
What classification code is assigned to this device?
This device is registered under product classification code MDB.
Similar Classification Devices (MDB)
Other Devices by BIOMERIEUX , INC.
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