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"Bausch & Brown" IOL guide (unsterilized) - Taiwan Registration 93103f7231ef7881851bd521fd1643b1

Access comprehensive regulatory information for "Bausch & Brown" IOL guide (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 93103f7231ef7881851bd521fd1643b1 and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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93103f7231ef7881851bd521fd1643b1
Registration Details
Taiwan FDA Registration: 93103f7231ef7881851bd521fd1643b1
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Device Details

"Bausch & Brown" IOL guide (unsterilized)
TW: โ€œๅšๅฃซๅ€ซโ€ไบบๅทฅๆฐดๆ™ถ้ซ”ๅฐŽๅผ•ๅ™จ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1

Registration Details

93103f7231ef7881851bd521fd1643b1

DHA04400941706

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

import

Dates and Status

Oct 27, 2010

Oct 27, 2025