REGULATION (EU) 2017/745 CE MDR
REGULATION (EU) 2017/745 CE MDR
Achieving compliance with EU medical device regulations is a significant accomplishment for Shyi Shin, as it allows our products to be freely sold and used in the EU market, while also showcasing our company's commitment to producing products of the highest quality and safety standards.
2023 / 03
30
ISO 13485
ISO 13485
ISO 13485 ASR Certification Number : 9211
ISO 13485 is an internationally recognized standard for quality management systems (QMS) specific to the medical device industry. 
2022 / 12
01
B2B Taiwan Trade
B2B Taiwan Trade
Officially launched the B2B platform of Taiwantrade.com, where you can browse and obtain more information about our company.
2022 / 05
06
SHYICARE
SHYICARE
Brand New Trademark Officially Launched
2022 / 02
17
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