Taiwan FDA registration ca38669bd60070193c359b166f49c240
Baijie M100 multi-function inspection system
TW: 百捷M100多功能檢驗系統
Taiwan·Risk Class 2·Qinli Biotechnology Co., Ltd. new tree factory·Registered Dec 09, 2014 – Dec 09, 2019CancelledRegistration details
- Analysis ID
- ca38669bd60070193c359b166f49c240
Company information
- Manufacturer
- Qinli Biotechnology Co., Ltd. new tree factory
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- GENERAL LIFE BIOTECHNOLOGY CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1775 Uric acid testing system;; A.1345 Glucose Test System;; A.1175 Cholesterol (Total) Testing System
- Import Information
- Domestic
Dates and status
- Registration Date
- Dec 09, 2014
- Expiry Date
- Dec 09, 2019
- Cancellation Date
- May 19, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Baijie M100 multi-function inspection system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca38669bd60070193c359b166f49c240 and manufactured by Qinli Biotechnology Co., Ltd. new tree factory. The authorized representative in Taiwan is GENERAL LIFE BIOTECHNOLOGY CO., LTD..
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