Taiwan FDA registration 0c3f2f9e4b5381c3bcae113a854c099a
"Japanese machine installation" dialysate supply device for many people
TW: “日機裝”多人數用透析液供給裝置
Taiwan·Risk Class 2·NIKKISO CO.,LTD. Shizuoka Medical Factory Shizuoka Plant·Registered May 30, 2007 – May 30, 2017CancelledRegistration details
- Analysis ID
- 0c3f2f9e4b5381c3bcae113a854c099a
- Customs Code
- DHA00601810201
Company information
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN NIKKISO CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- import
Dates and status
- Registration Date
- May 30, 2007
- Expiry Date
- May 30, 2017
- Cancellation Date
- Dec 14, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Japanese machine installation" dialysate supply device for many people in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0c3f2f9e4b5381c3bcae113a854c099a and manufactured by NIKKISO CO.,LTD. Shizuoka Medical Factory Shizuoka Plant. The authorized representative in Taiwan is TAIWAN NIKKISO CO., LTD..
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