gudid
Primary ID: 280021
AST Inoculator (UDI 280021)
Manufactured by Selux Diagnostics, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for AST Inoculator - Primary ID 280021
Device Regulatory Overview
The AST Inoculator (Model/Catalog Number: 280021) is a medical device manufactured by Selux Diagnostics, Inc.. This product is indexed under FDA Product Code / Category Classification LON within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 280021
- Product Code / EMDN
- LON
- Device Name
- Database Sync Date
- 2026-08-09 09:37:43
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 AST Inoculator?
The registered manufacturer of record for AST Inoculator is Selux Diagnostics, Inc..
What is the Primary UDI-DI identifier for AST Inoculator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 280021.
What classification code is assigned to this device?
This device is registered under product classification code LON.
Similar Classification Devices (LON)
Other Devices by Selux Diagnostics, Inc.
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