Taiwan FDA registration 5f81815624da9bffc47a6a7002c542b4
Nipro Synthetic Hemodialyzer
TW: “尼普洛”血液透析過濾器
Taiwan·Risk Class 2·MD·Nipro Corporation Odate Factory·Registered Sep 15, 2017 – Sep 15, 2027ActiveRegistration details
- Analysis ID
- 5f81815624da9bffc47a6a7002c542b4
- License Form
- Ministry of Health Medical Device Import No. 030228
- Customs Code
- DHA05603022801
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
- Sep 15, 2017
- Expiry Date
- Sep 15, 2027
About this record
Access comprehensive regulatory information for Nipro Synthetic Hemodialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f81815624da9bffc47a6a7002c542b4 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