"Bausch & Lomb" diamond-regulated intraocular lens - Taiwan Registration 5df1ab04fbc9aa5602f480add8b2447e
Access comprehensive regulatory information for "Bausch & Lomb" diamond-regulated intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5df1ab04fbc9aa5602f480add8b2447e and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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
For details, it is Chinese approved copy of the imitation order
M Ophthalmology
M.3600 Artificial Crystal
import
Dates and Status
Sep 02, 2010
Sep 02, 2020
May 19, 2022
Cancellation Information
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