gudid
Primary ID: A-03
N/A (UDI A-03)
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 A-03
Device Regulatory Overview
The N/A (Model/Catalog Number: A-03) is a medical device manufactured by HARDY DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification LXH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- A-03
- Product Code / EMDN
- LXH
- Device Name
- Blood Agar EH, 5%, 15x100mm Plate, 17mlHardy Diagnostics Blood Agar Enhanced Hemolysis (EH) is recommended for use as a general purpose growth medium for the isolation, cultivation, and differentiation of fastidious microorganisms from specimens where clear and distinct hemolytic reactions are of prime importance.
- Database Sync Date
- 2026-08-09 09:12:11
Full Regulatory Attributes
🔒 Token Gated
{
"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 A-03.
What classification code is assigned to this device?
This device is registered under product classification code LXH.
Similar Classification Devices (LXH)
Other Devices by HARDY DIAGNOSTICS
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