gudid
Primary ID: BACT/ALERT BPA
BACT/ALERT BPA (UDI BACT/ALERT BPA)
Manufactured by BIOMERIEUX , INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BACT/ALERT BPA - Primary ID BACT/ALERT BPA
Device Regulatory Overview
The BACT/ALERT BPA (Model/Catalog Number: BACT/ALERT BPA) is a medical device manufactured by BIOMERIEUX , INC.. This product is indexed under FDA Product Code / Category Classification MZC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BACT/ALERT BPA
- Product Code / EMDN
- MZC
- Device Name
- BacT/ALERT BPA (aerobic culture) bottles are used for QC testing of leukocyte reduced apheresis platelet units,leukocyte reduced single units of whole blood platelet concentrates
- 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 BPA?
The registered manufacturer of record for BACT/ALERT BPA is BIOMERIEUX , INC..
What is the Primary UDI-DI identifier for BACT/ALERT BPA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BACT/ALERT BPA.
What classification code is assigned to this device?
This device is registered under product classification code MZC.
Similar Classification Devices (MZC)
Other Devices by BIOMERIEUX , INC.
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