"Pentax" light source and accessories (unsterilized) - Taiwan Registration 1df2a7bb4878b6f5679f584b1da5a6c7
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 1df2a7bb4878b6f5679f584b1da5a6c7 and manufactured by PENTAX CORPORATION. The authorized representative in Taiwan is WHOLE WELL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA 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
Apr 10, 2006
Apr 10, 2011
Jul 25, 2014
Cancellation Information
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