gudid
Primary ID: VITEK 2 AST-N804
VITEK 2 AST-N804 (UDI VITEK 2 AST-N804)
Manufactured by BIOMERIEUX , INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VITEK 2 AST-N804 - Primary ID VITEK 2 AST-N804
Device Regulatory Overview
The VITEK 2 AST-N804 (Model/Catalog Number: VITEK 2 AST-N804) is a medical device manufactured by BIOMERIEUX , INC.. This product is indexed under FDA Product Code / Category Classification LON within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- VITEK 2 AST-N804
- Product Code / EMDN
- LON
- Device Name
- VITEK 2 Gram Negative Susceptibility Card is intended for use with the VITEK 2 Systems to determine the susceptibility of clinically significant aerobic gram-negative bacilli
- 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 VITEK 2 AST-N804?
The registered manufacturer of record for VITEK 2 AST-N804 is BIOMERIEUX , INC..
What is the Primary UDI-DI identifier for VITEK 2 AST-N804?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VITEK 2 AST-N804.
What classification code is assigned to this device?
This device is registered under product classification code LON.
Similar Classification Devices (LON)
Other Devices by BIOMERIEUX , INC.
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