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"Bausch & Lomb" diamond-regulated intraocular lens - Taiwan Registration 5df1ab04fbc9aa5602f480add8b2447e

Access comprehensive regulatory information for "Bausch & Lomb" diamond-regulated intraocular lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 5df1ab04fbc9aa5602f480add8b2447e 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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5df1ab04fbc9aa5602f480add8b2447e
Registration Details
Taiwan FDA Registration: 5df1ab04fbc9aa5602f480add8b2447e
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Device Details

"Bausch & Lomb" diamond-regulated intraocular lens
TW: โ€œๅšๅฃซๅ€ซโ€ๆ™ถ้‘ฝ่ชฟ็ฏ€ๅผไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
Cancelled

Registration Details

5df1ab04fbc9aa5602f480add8b2447e

DHA00602142101

Company Information

United States

Product Details

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

M Ophthalmology

M.3600 Artificial Crystal

import

Dates and Status

Sep 02, 2010

Sep 02, 2020

May 19, 2022

Cancellation Information

Logged out

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