Taiwan FDA registration f8cf9536a58853b4567ca7fb9fbbe998

“Fresenius” Blunt Fistula Needles

TW: “費森尤斯”瘻管針
Taiwan flagTaiwan·Risk Class 2·MD·Nipro (Thailand) Corporation Limited·Registered Oct 06, 2014 – Oct 06, 2019Cancelled
Registration details
Analysis ID
f8cf9536a58853b4567ca7fb9fbbe998
License Form
Ministry of Health Medical Device Import No. 026633
Customs Code
DHA05602663308
Company information
Manufacturer Country
Thailand
Product details
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
Oct 06, 2014
Expiry Date
Oct 06, 2019
Cancellation Date
Jun 16, 2022
Cancellation information
Status
Logged out
Reason
許可證已逾有效期未申請展延
About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices