Creatinine-Colorimetric (UDI G458235001YJ)
Manufactured by Spectrum for Diagnostic Industries (Joint Stock Company)
Device Regulatory Overview
The Creatinine-Colorimetric (Model/Catalog Number: 235 001) is a medical device manufactured by Spectrum for Diagnostic Industries (Joint Stock Company). This product is indexed under FDA Product Code / Category Classification W01010207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 235 001
- Product Code / EMDN
- W01010207
- Device Name
- Creatinine-Colorimetric
- Database Sync Date
- 2026-08-09 16:58:33
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 Creatinine-Colorimetric?
The registered manufacturer of record for Creatinine-Colorimetric is Spectrum for Diagnostic Industries (Joint Stock Company).
What is the Primary UDI-DI identifier for Creatinine-Colorimetric?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G458235001YJ.
What classification code is assigned to this device?
This device is registered under product classification code W01010207.
Similar Classification Devices (W01010207)
Other Devices by Spectrum for Diagnostic Industries (Joint Stock Company)
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