"Pentax" light source and accessories (unsterilized) - Taiwan Registration 5eb86c3cf63e83ae4dde0151292218dc
Access comprehensive regulatory information for "Pentax" light source and accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5eb86c3cf63e83ae4dde0151292218dc and manufactured by HOYA CORPORATION. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PENTAX CORPORATION, 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
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
G ENT Science
G.4350 Ear, nose and throat optical fiber light sources and carriers
import
Dates and Status
Mar 04, 2013
Mar 04, 2023