Uric acid - Liquizyme Uricase-PAP (Single Reagent) (UDI G4583230038H)
Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)
Device Regulatory Overview
The Uric acid - Liquizyme Uricase-PAP (Single Reagent) (Model/Catalog Number: 323 003) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010231 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 323 003
- Product Code / EMDN
- W01010231
- Device Name
- Uric acid - Liquizyme Uricase-PAP (Single Reagent)
- Database Sync Date
- 2026-08-09 17:14:56
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 - Liquizyme Uricase-PAP (Single Reagent)?
The registered manufacturer of record for Uric acid - Liquizyme Uricase-PAP (Single Reagent) is Spectrum for Diagnostic Industries (Joint Stock Company).
What is the Primary UDI-DI identifier for Uric acid - Liquizyme Uricase-PAP (Single Reagent)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G4583230038H.
What classification code is assigned to this device?
This device is registered under product classification code W01010231.
Similar Classification Devices (W01010231)
Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)
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