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“Fresenius” Blunt Fistula Needles - Taiwan Registration f8cf9536a58853b4567ca7fb9fbbe998

Access comprehensive regulatory information for “Fresenius” Blunt Fistula Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f8cf9536a58853b4567ca7fb9fbbe998 and manufactured by Nipro (Thailand) Corporation Limited. The authorized representative in Taiwan is FRESENIUS MEDICAL CARE TAIWAN 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.

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f8cf9536a58853b4567ca7fb9fbbe998
Registration Details
Taiwan FDA Registration: f8cf9536a58853b4567ca7fb9fbbe998
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Device Details

“Fresenius” Blunt Fistula Needles
TW: “費森尤斯”瘻管針
Risk Class 2
MD
Cancelled

Registration Details

f8cf9536a58853b4567ca7fb9fbbe998

Ministry of Health Medical Device Import No. 026633

DHA05602663308

Company Information

Product Details

H Gastroenterology-urology devices

H5540 Blood access devices and accessories

Imported from abroad

Dates and Status

Oct 06, 2014

Oct 06, 2019

Jun 16, 2022

Cancellation Information

Logged out

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