Taiwan FDA registration f6b9d5953d5cc28b4bba0e88ee411436

"Nipro" hollow fiber dialysis cylinder

TW: “尼普洛”中空纖維透析筒
Taiwan flagTaiwan·Risk Class 2·Nipro Corporation Odate Factory·Registered Mar 15, 2010 – Mar 15, 2020Cancelled
Registration details
Analysis ID
f6b9d5953d5cc28b4bba0e88ee411436
Customs Code
DHA00602066804
Company information
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
import
Dates and status
Registration Date
Mar 15, 2010
Expiry Date
Mar 15, 2020
Cancellation Date
Jun 07, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
Companies making similar products

Top companies providing products similar to ""Nipro" hollow fiber dialysis cylinder"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Nipro" hollow fiber dialysis cylinder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f6b9d5953d5cc28b4bba0e88ee411436 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, 2 companies making similar products including NIPRO CORPORATION ODATE FACTORY, Nipro Corporation Odate Factory, and 3 recent registrations in the same category. 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+ Devices2 Competitors3 Recent Registrations