"Fujifilm" rinses the electric knife with high frequency in a single time - Taiwan Registration 12e52e96dccd3ab1056dc38a293e0204
Access comprehensive regulatory information for "Fujifilm" rinses the electric knife with high frequency in a single time in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12e52e96dccd3ab1056dc38a293e0204 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE 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.
Device Details
Product Details
Details are as detailed as approved Chinese instructions
H Gastroenterology and urology
H.4300 Electrosurgical device for endoscopy and accessories thereof
import
Dates and Status
Jul 15, 2022
Jul 15, 2027