Taiwan FDA registration 54068c1518dbd1381562bacdeeef78a7
"Nikki-ho" dialysis monitoring device
TW: “日機裝”透析用監視裝置
Taiwan·Risk Class 2·NIKKISO CO., LTD. SHIZUOKA MEDICAL FACTORY SHIZUOKA PLANT·Registered May 24, 2007 – May 24, 2017CancelledRegistration details
- Analysis ID
- 54068c1518dbd1381562bacdeeef78a7
- Customs Code
- DHA00601809708
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 24, 2007
- Expiry Date
- May 24, 2017
- Cancellation Date
- Nov 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Nikki-ho" dialysis monitoring device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 54068c1518dbd1381562bacdeeef78a7 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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