"Japanese Medical" low-frequency therapy device - Taiwan Registration d51160b31afaeaa7edb6cbb506f7c4b9

Access comprehensive regulatory information for "Japanese Medical" low-frequency therapy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d51160b31afaeaa7edb6cbb506f7c4b9 and manufactured by Nihon Medix Co., Ltd. Kashiwa Factory;; DIGI I's Ltd.. The authorized representative in Taiwan is CROWNMED ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NIHON MEDIX CO., LTD. KASHIWA FACTORY, and 1 recent registrations in the same category. 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.