Aspartate aminotransferase (AST/GOT) UV-Kinetic (4+1) (UDI G45817302020EN)
Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)
Device Regulatory Overview
The Aspartate aminotransferase (AST/GOT) UV-Kinetic (4+1) (Model/Catalog Number: 173 02 020) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 173 02 020
- Product Code / EMDN
- W01010110
- Device Name
- Aspartate aminotransferase (AST/GOT) UV-Kinetic
- Database Sync Date
- 2026-08-09 16:50:37
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 Aspartate aminotransferase (AST/GOT) UV-Kinetic (4+1)?
The registered manufacturer of record for Aspartate aminotransferase (AST/GOT) UV-Kinetic (4+1) is Spectrum for Diagnostic Industries (Joint Stock Company).
What is the Primary UDI-DI identifier for Aspartate aminotransferase (AST/GOT) UV-Kinetic (4+1)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G45817302020EN.
What classification code is assigned to this device?
This device is registered under product classification code W01010110.
Similar Classification Devices (W01010110)
Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)
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