gudid
Primary ID: W20
N/A (UDI W20)
Manufactured by HARDY DIAGNOSTICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID W20
Device Regulatory Overview
The N/A (Model/Catalog Number: W20) is a medical device manufactured by HARDY DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification JSG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- W20
- Product Code / EMDN
- JSG
- Device Name
- Emmon's Sabdex (Sabouraud Dextrose) Agar, deep fill, 15x100mm plate, order by the package of 10Emmons Sabdex agar is recommended for the isolation, cultivation, and maintenance of non-pathogenic and pathogenic species of fungi and yeasts.
- Database Sync Date
- 2026-08-09 09:31:30
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 N/A?
The registered manufacturer of record for N/A is HARDY DIAGNOSTICS.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W20.
What classification code is assigned to this device?
This device is registered under product classification code JSG.
Similar Classification Devices (JSG)
Other Devices by HARDY DIAGNOSTICS
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