Taiwan FDA registration c02ad7629b24f9dd1eab16e6e198d676
AXA Clinical Chemistry Analyzer (Unsterilized)
TW: "安盛" 臨床化學分析儀 (未滅菌)
Registration details
- Analysis ID
- c02ad7629b24f9dd1eab16e6e198d676
Company information
- Manufacturer
- PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- IXENSOR CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of "centrifugal biochemical analyzer for clinical use (A.2140)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2140 Centrifugal biochemistry analyzer for clinical use
- Import Information
- QMS/QSD;; 國產;; 委託製造
Dates and status
- Registration Date
- Jul 01, 2016
- Expiry Date
- Jul 01, 2021
- Cancellation Date
- Dec 21, 2017
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for AXA Clinical Chemistry Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c02ad7629b24f9dd1eab16e6e198d676 and manufactured by PROTECTLIFE INTERNATIONAL BIOMEDICAL INC.. The authorized representative in Taiwan is IXENSOR CO., LTD..
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