Lactate dehydrogenase(LDH) UV- Kinetic (4+1) (UDI G458185020208P)
Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)
Device Regulatory Overview
The Lactate dehydrogenase(LDH) UV- Kinetic (4+1) (Model/Catalog Number: 185 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 W01010120 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 185 02 020
- Product Code / EMDN
- W01010120
- Device Name
- Lactate dehydrogenase(LDH) UV- Kinetic
- Database Sync Date
- 2026-08-09 17:15:46
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 Lactate dehydrogenase(LDH) UV- Kinetic (4+1)?
The registered manufacturer of record for Lactate dehydrogenase(LDH) UV- Kinetic (4+1) is Spectrum for Diagnostic Industries (Joint Stock Company).
What is the Primary UDI-DI identifier for Lactate dehydrogenase(LDH) UV- Kinetic (4+1)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G458185020208P.
What classification code is assigned to this device?
This device is registered under product classification code W01010120.
Similar Classification Devices (W01010120)
Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)
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