Pure Global

“Kawasumi Laboratories” Hollow Fiber Dialyzer - Taiwan Registration efa6b8da2f6dfb115f73dcdd902bd10b

Access comprehensive regulatory information for “Kawasumi Laboratories” Hollow Fiber Dialyzer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number efa6b8da2f6dfb115f73dcdd902bd10b and manufactured by KAWASUMI LABORATORIES,INC. MIE FACTORY. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..

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 Database
Powered by Pure Global AI
89,000+ Devices
efa6b8da2f6dfb115f73dcdd902bd10b
Registration Details
Taiwan FDA Registration: efa6b8da2f6dfb115f73dcdd902bd10b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Kawasumi Laboratories” Hollow Fiber Dialyzer
TW: “川澄化工”人工腎臟
Risk Class 2
MD
Cancelled

Registration Details

efa6b8da2f6dfb115f73dcdd902bd10b

Ministry of Health Medical Device Import No. 026794

DHA05602679406

Company Information

Product Details

H Gastroenterology-urology devices

H5820 Hemodialysis systems and accessories

Imported from abroad

Dates and Status

Nov 25, 2014

Nov 25, 2019

May 19, 2022

Cancellation Information

Logged out

許可證逾有效期未申請展延