Taiwan FDA registration ee95a9777bd0ba80c68fe15b0a2f2853

HSING HO HEMODIALYSIS BLOOD TUBING SET

TW: 杏合血液迴路管

Taiwan·Risk Class 2·MD·Xinghe Biomedical Co., Ltd. Taichung Factory·Registered Aug 03, 2015 – Aug 03, 2020Cancelled

Registration details

Analysis ID: ee95a9777bd0ba80c68fe15b0a2f2853
License Form: Ministry of Health Medical Device Manufacturing No. 005057

Company information

Manufacturer: Xinghe Biomedical Co., Ltd. Taichung Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: Xinghe Biomedical Co., Ltd. Taichung Factory

Product details

Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H5820 Hemodialysis systems and accessories
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 03, 2015
Expiry Date: Aug 03, 2020
Cancellation Date: Aug 05, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for HSING HO HEMODIALYSIS BLOOD TUBING SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ee95a9777bd0ba80c68fe15b0a2f2853 and manufactured by Xinghe Biomedical Co., Ltd. Taichung Factory. The authorized representative in Taiwan is Xinghe Biomedical Co., Ltd. Taichung Factory.

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