gudid
Primary ID: BACT/ALERT MP
BACT/ALERT MP (UDI BACT/ALERT MP)
Manufactured by BIOMERIEUX , INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BACT/ALERT MP - Primary ID BACT/ALERT MP
Device Regulatory Overview
The BACT/ALERT MP (Model/Catalog Number: BACT/ALERT MP) 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 MP
- Product Code / EMDN
- MDB
- Device Name
- Mycobacteria Detection bottle for recovery and detection of mycobacteria from sterile body specimens other than blood, and from digested-decontaminated clinical specimens.
- Database Sync Date
- 2026-08-09 09:46:56
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BACT/ALERT MP?
The registered manufacturer of record for BACT/ALERT MP is BIOMERIEUX , INC..
What is the Primary UDI-DI identifier for BACT/ALERT MP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BACT/ALERT MP.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint