Alkaline Phosphatase (ALP) - Liquizyme (4+1) IFCC (UDI G45815810010SM)
Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)
Device Regulatory Overview
The Alkaline Phosphatase (ALP) - Liquizyme (4+1) IFCC (Model/Catalog Number: 158 10 010) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 158 10 010
- Product Code / EMDN
- W01010105
- Device Name
- Alkaline phosphatase (ALP) Kinetic - IFCC
- Database Sync Date
- 2026-08-09 16:29:27
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 Alkaline Phosphatase (ALP) - Liquizyme (4+1) IFCC?
The registered manufacturer of record for Alkaline Phosphatase (ALP) - Liquizyme (4+1) IFCC is Spectrum for Diagnostic Industries (Joint Stock Company).
What is the Primary UDI-DI identifier for Alkaline Phosphatase (ALP) - Liquizyme (4+1) IFCC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G45815810010SM.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)
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