gudid
Primary ID: K38
NA (UDI K38)
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 K38
Device Regulatory Overview
The NA (Model/Catalog Number: K38) 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
- K38
- Product Code / EMDN
- JTZ
- Device Name
- MUELLER HINTON BROTHFor the preparation of suspensions for disk diffusion sensitivity testing.
- 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 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 K38.
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
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