Taiwan FDA registration f36032ab1f4f8130bb9bcdedf04187eb

Jiadak blood glucose monitoring system

TW: 嘉測克血糖監測系統
Taiwan flagTaiwan·Risk Class 2·OK BIOTECH CO., LTD.·Registered Jul 27, 2021 – Aug 27, 2026Active
Registration details
Analysis ID
f36032ab1f4f8130bb9bcdedf04187eb
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
OK BIOTECH CO., LTD.
Product details
Intended Use
This product is only for in vitro testing, quantitatively detecting the blood glucose value of fresh microvascular whole blood from fingertips and other blood collection sites (palm, forearm, upper arm, calf and thigh), and is not suitable for neonatal testing. This product can be used by professional medical professionals or diabetic patients to measure blood glucose levels, and is not intended as the final diagnosis of diabetes.
Product Type (Level 1)
A Clinical Chemistry and Clinical Toxicology;; I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4800 Manual instruments for general surgery; A.1345 Glucose Test System
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Jul 27, 2021
Expiry Date
Aug 27, 2026
About this record

Access comprehensive regulatory information for Jiadak blood glucose monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f36032ab1f4f8130bb9bcdedf04187eb and manufactured by OK BIOTECH CO., LTD.. The authorized representative in Taiwan is OK BIOTECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free DatabasePowered by Pure Global AI89,000+ Devices