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"Bausch & Len" IOL Guides (Sterile/Unsterile) - Taiwan Registration 0e618625ad164e60c29e54488fcd435c

Access comprehensive regulatory information for "Bausch & Len" IOL Guides (Sterile/Unsterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0e618625ad164e60c29e54488fcd435c 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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0e618625ad164e60c29e54488fcd435c
Registration Details
Taiwan FDA Registration: 0e618625ad164e60c29e54488fcd435c
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Device Details

"Bausch & Len" IOL Guides (Sterile/Unsterile)
TW: "ๅšๅฃซๅ€ซ" ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ(ๆป…่Œ/ๆœชๆป…่Œ)
Risk Class 1

Registration Details

0e618625ad164e60c29e54488fcd435c

DHA09402308001

Company Information

United States

Product Details

Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.

M Ophthalmology

M.4300 Artificial crystal body inducer

Input;; QMS/QSD

Dates and Status

Mar 24, 2023

Mar 24, 2028