GUDIDData
gudid Primary ID: H57

N/A (UDI H57)

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 H57

Device Regulatory Overview

The N/A (Model/Catalog Number: H57) 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
H57
Product Code / EMDN
JSG
Device Name
Malt Extract Agar, 15x150mm Plate, 68ml. Hardy Diagnostics Malt Extract Agar is recommended for the cultivation, isolation, and maintenance of yeasts and molds.
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 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 H57.

What classification code is assigned to this device?

This device is registered under product classification code JSG.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint