gudid
Primary ID: 12-U7581-120
Uric Acid (UDI 12-U7581-120)
Manufactured by HORIBA INSTRUMENTS INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Uric Acid - Primary ID 12-U7581-120
Device Regulatory Overview
The Uric Acid (Model/Catalog Number: 12-U7581-120) is a medical device manufactured by HORIBA INSTRUMENTS INCORPORATED. This product is indexed under FDA Product Code / Category Classification KNK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 12-U7581-120
- Product Code / EMDN
- KNK
- Device Name
- For the quantitative determination of Uric Acid in serum. For in vitro diagnostic use only.
- Database Sync Date
- 2026-08-09 09:22:13
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 Uric Acid?
The registered manufacturer of record for Uric Acid is HORIBA INSTRUMENTS INCORPORATED.
What is the Primary UDI-DI identifier for Uric Acid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12-U7581-120.
What classification code is assigned to this device?
This device is registered under product classification code KNK.
Similar Classification Devices (KNK)
Other Devices by HORIBA INSTRUMENTS INCORPORATED
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