Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II (UDI 06936983164849)
Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.
Device Regulatory Overview
The Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II (Model/Catalog Number: AGKUCR-200ST10) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0201069099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AGKUCR-200ST10
- Product Code / EMDN
- W0201069099
- Device Name
- Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II
- Database Sync Date
- 2026-08-09 16:58:29
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 Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II?
The registered manufacturer of record for Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II is Hangzhou Alltest Biotech.Co.,Ltd..
What is the Primary UDI-DI identifier for Blood Glucose/ Ketone/ Uric Acid/ Total Cholesterol 4 in 1 monitoring system II?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936983164849.
What classification code is assigned to this device?
This device is registered under product classification code W0201069099.
Similar Classification Devices (W0201069099)
Other Devices by Hangzhou Alltest Biotech.Co.,Ltd.
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