Taiwan FDA registration 12a52f7002c154f6e8fbeb748f1d6bfb
“Nipro” Hemodialyzer
TW: “尼普洛”中空纖維透析筒
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Dec 20, 2018 – Dec 20, 2028ActiveRegistration details
- Analysis ID
- 12a52f7002c154f6e8fbeb748f1d6bfb
- License Form
- Ministry of Health Medical Device Import No. 031932
- Customs Code
- DHA05603193202
Company information
- Manufacturer
- Nipro Corporation Odate Factory
- Manufacturer Country
- Japan
- Authorized Representative
- HUA CHIANG MEDICAL CO., LTD.
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
- Imported from abroad
Dates and status
- Registration Date
- Dec 20, 2018
- Expiry Date
- Dec 20, 2028
About this record
Access comprehensive regulatory information for “Nipro” Hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12a52f7002c154f6e8fbeb748f1d6bfb and manufactured by Nipro Corporation Odate Factory. The authorized representative in Taiwan is HUA CHIANG MEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices