gudid
Primary ID: G345
NA (UDI G345)
Manufactured by HARDY DIAGNOSTICS
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID G345
Device Regulatory Overview
The NA (Model/Catalog Number: G345) is a medical device manufactured by HARDY DIAGNOSTICS. This product is indexed under FDA Product Code / Category Classification JTZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- G345
- Product Code / EMDN
- JTZ
- Device Name
- MUELLER HINTON AGAR, 20mlNot intended for disk diffusion testing. For the cultivation of microorganisms.
- Database Sync Date
- 2026-08-09 09:31:30
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of NA?
The registered manufacturer of record for NA is HARDY DIAGNOSTICS.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G345.
What classification code is assigned to this device?
This device is registered under product classification code JTZ.
Similar Classification Devices (JTZ)
Other Devices by HARDY DIAGNOSTICS
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint