"Dr. Len" Ruilin Dual Action Wetting Solution - Taiwan Registration 80afcf71a9fc86322e1ba13ae8543725
Access comprehensive regulatory information for "Dr. Len" Ruilin Dual Action Wetting Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 80afcf71a9fc86322e1ba13ae8543725 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.
Free Database
Powered by Pure Global AI
89,000+ Devices
80afcf71a9fc86322e1ba13ae8543725
Registration Details
Taiwan FDA Registration: 80afcf71a9fc86322e1ba13ae8543725
Device Details
"Dr. Len" Ruilin Dual Action Wetting Solution
TW: โๅๅฃซๅซโ็้้ๆๆฝคๆฟๆถฒ
Risk Class 2

