"Taiwan tower" anterior chamber catheter (sterilized) - Taiwan Registration 42e7553e9dbda7c97c46cb6fcba1f32d
Access comprehensive regulatory information for "Taiwan tower" anterior chamber catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42e7553e9dbda7c97c46cb6fcba1f32d and manufactured by PSI/EYE-KO, Inc. dba Anodyne Surgical. The authorized representative in Taiwan is TAIWAN SANTEN PHARMACEUTICAL 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
Limited to the first level identification scope of the "Manual Ophthalmic Surgical Instruments (M.4350)" of the Measures for the Classification and Grading of Medical Equipment.
M Ophthalmology
M.4350 ๆๅๅผ็ผ็งๆ่กๅจๆขฐ
QMS/QSD;; ่ผธๅ ฅ
Dates and Status
Jun 21, 2023
Jun 21, 2028