Taiwan FDA registration 481ba9e4ab795d905dddf0dc4c8cee7b
“BenQ” Qflux Dialyzer
TW: “明基”血液透析器
Taiwan·Risk Class 2·MD·BENQ DIALYSIS TECHNOLOGY CORP.·Registered Dec 13, 2017 – Dec 13, 2027ActiveRegistration details
- Analysis ID
- 481ba9e4ab795d905dddf0dc4c8cee7b
- License Form
- Ministry of Health Medical Device Manufacturing No. 006010
Company information
- Manufacturer
- BENQ DIALYSIS TECHNOLOGY CORP.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BENQ DIALYSIS TECHNOLOGY CORP.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H5860 Highly permeable hemodialysis system
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Dec 13, 2017
- Expiry Date
- Dec 13, 2027
About this record
Access comprehensive regulatory information for “BenQ” Qflux Dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 481ba9e4ab795d905dddf0dc4c8cee7b and manufactured by BENQ DIALYSIS TECHNOLOGY CORP.. The authorized representative in Taiwan is BENQ DIALYSIS TECHNOLOGY CORP..
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