gudid
Primary ID: J330
N/A (UDI J330)
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 J330
Device Regulatory Overview
The N/A (Model/Catalog Number: J330) 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
- J330
- Product Code / EMDN
- JSG
- Device Name
- TSA / CET (Cetrimide Selective Agar) / MSA (Mannitol Salt Agar), USP, 15x100mm Triplate, 7ml/section. Hardy Diagnostics Cetrimide Selective Agar is recommended for the selective isolation and identification of Pseudomonas aeruginosa. Hardy Diagnostics Mannitol Salt Agar (MSA) is recommended for use as a selective and differential medium for the isolation of pathogenic staphylococci. Hardy Diagnostics Tryptic Soy Agar (TSA), USP is recommended for use as a general growth medium for the detection and enumeration of microorganisms from non-clinical samples.
- 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 J330.
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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