Taiwan FDA registration 4b25d700175d8e321f8ddae7d901ecaf
“Nipro” Blood Tubing set for Hemodialysis (Gamma Irradiation)
TW: “尼普洛”透析用迴路(Gamma滅菌)
Taiwan·Risk Class 2·MD·Nipro (Thailand) Corporation Limited·Registered Sep 19, 2017 – Sep 19, 2027ActiveRegistration details
- Analysis ID
- 4b25d700175d8e321f8ddae7d901ecaf
- License Form
- Ministry of Health Medical Device Import No. 030236
- Customs Code
- DHA05603023600
Company information
- Manufacturer
- Nipro (Thailand) Corporation Limited
- Manufacturer Country
- Thailand
- 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)
- H5540 Blood access devices and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 19, 2017
- Expiry Date
- Sep 19, 2027
About this record
Access comprehensive regulatory information for “Nipro” Blood Tubing set for Hemodialysis (Gamma Irradiation) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4b25d700175d8e321f8ddae7d901ecaf and manufactured by Nipro (Thailand) Corporation Limited. 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