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"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.

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80afcf71a9fc86322e1ba13ae8543725
Registration Details
Taiwan FDA Registration: 80afcf71a9fc86322e1ba13ae8543725
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Device Details

"Dr. Len" Ruilin Dual Action Wetting Solution
TW: โ€œๅšๅฃซๅ€ซโ€็‘ž้œ–้›™ๆ•ˆๆฝคๆฟ•ๆถฒ
Risk Class 2

Registration Details

80afcf71a9fc86322e1ba13ae8543725

DHA00602160103

Company Information

United States

Product Details

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

M Ophthalmology

M.5928 Products for the preservation of soft contact lenses

import

Dates and Status

Oct 22, 2010

Oct 22, 2025