Taiwan FDA registration 3e5bd4c216f1ea1b7429af912694c287
"Japanese machine-mounted" hollow fibrous hemodialysis tube
TW: "日機裝" 中空纖維型血液透析筒
Taiwan·Risk Class 2·NIKKISO CO., LTD., KANAZAWA PLANT·Registered Nov 13, 2003 – Nov 13, 2018CancelledRegistration details
- Analysis ID
- 3e5bd4c216f1ea1b7429af912694c287
- Customs Code
- DHA00601046306
Company information
- Manufacturer
- NIKKISO CO., LTD., KANAZAWA PLANT
- Manufacturer Country
- Japan
- Authorized Representative
- TAIWAN NIKKISO CO., LTD.
Product details
- Product Type (Level 1)
- H Gastroenterology and urology
- Import Information
- import
Dates and status
- Registration Date
- Nov 13, 2003
- Expiry Date
- Nov 13, 2018
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Japanese machine-mounted" hollow fibrous hemodialysis tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3e5bd4c216f1ea1b7429af912694c287 and manufactured by NIKKISO CO., LTD., KANAZAWA PLANT. The authorized representative in Taiwan is TAIWAN NIKKISO CO., LTD..
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