"Dr. Len" posterior chamber vitrectomy surgical kit - Taiwan Registration 36ba558c73266279b0a873c880131e67
Access comprehensive regulatory information for "Dr. Len" posterior chamber vitrectomy surgical kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 36ba558c73266279b0a873c880131e67 and manufactured by BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.
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Device Details
Product Details
For details, it is Chinese approved copy of the imitation order
M Ophthalmology
M.4150 Vitreous Suction and Cutting Apparatus
import
Dates and Status
May 15, 2009
May 15, 2019
May 19, 2022
Cancellation Information
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