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"Bausch & Len" Brighton New Cleansing Multi-functional Solution - Taiwan Registration 3df1e50bce17de1e68cd3436bd33ed7a

Access comprehensive regulatory information for "Bausch & Len" Brighton New Cleansing Multi-functional Solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3df1e50bce17de1e68cd3436bd33ed7a 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.

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3df1e50bce17de1e68cd3436bd33ed7a
Registration Details
Taiwan FDA Registration: 3df1e50bce17de1e68cd3436bd33ed7a
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Device Details

"Bausch & Len" Brighton New Cleansing Multi-functional Solution
TW: โ€œๅšๅฃซๅ€ซโ€ๅš่ฆ–้ “ๆ–ฐๆฝ”ๅคšๅŠŸ่ƒฝ่ญท็†ๆถฒ
Risk Class 2

Registration Details

3df1e50bce17de1e68cd3436bd33ed7a

DHA00601973901

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order.

M Ophthalmology

M.5918 Rigid Breathable Contact Lens Preservation Products

import

Dates and Status

Mar 26, 2009

Mar 26, 2029