Taiwan FDA registration ed969ef279ec48d13ef965c123469f78
"Shibuya" Nipro personal dialysis device
TW: “澁谷”尼普洛個人用透析裝置
Registration details
- Analysis ID
- ed969ef279ec48d13ef965c123469f78
- Customs Code
- DHA05602531604
Company information
- Manufacturer
- Shibuya Corporation;; NIPRO CORPORATION
- 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 and urology
- Product Type (Level 2)
- H.5820 血液透析系統及其附件
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Aug 01, 2013
- Expiry Date
- Aug 01, 2028
About this record
Access comprehensive regulatory information for "Shibuya" Nipro personal dialysis device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ed969ef279ec48d13ef965c123469f78 and manufactured by Shibuya Corporation;; NIPRO CORPORATION. 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