gudid
Primary ID: VITEK2 AST-ST01
VITEK 2 AST-ST01 (UDI VITEK2 AST-ST01)
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-ST01 - Primary ID VITEK2 AST-ST01
Device Regulatory Overview
The VITEK 2 AST-ST01 (Model/Catalog Number: VITEK2 AST-ST01) 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
- VITEK2 AST-ST01
- Product Code / EMDN
- LON
- Device Name
- The VITEK 2 Streptococcus Susceptibility Card is intended for use with the VITEK 2 to determine the susceptibility of S. pneumo , beta-hemolytic Strep, & Viridans Strep
- 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-ST01?
The registered manufacturer of record for VITEK 2 AST-ST01 is BIOMERIEUX , INC..
What is the Primary UDI-DI identifier for VITEK 2 AST-ST01?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VITEK2 AST-ST01.
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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