"Fujifilm film" general photographic X-ray device - Taiwan Registration ce03865344b804d2ef1f67055fd89b72
Access comprehensive regulatory information for "Fujifilm film" general photographic X-ray device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ce03865344b804d2ef1f67055fd89b72 and manufactured by FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Corporation Medical System Operations Group, Kashiwa, 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.
Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
P Radiology Science
P.1680 ๅบๅฎๅผXๅ ็ณป็ตฑ
Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and Status
Jul 06, 2009
Jul 06, 2029