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"Dr. Len" Schuber intraocular lens - Taiwan Registration d6b302faff71b359c6bbd41bb26f88aa

Access comprehensive regulatory information for "Dr. Len" Schuber 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 d6b302faff71b359c6bbd41bb26f88aa and manufactured by BAUSCH & LOMB INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BAUSCH & LOMB INC., and 1 recent registrations in the same category. 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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d6b302faff71b359c6bbd41bb26f88aa
Registration Details
Taiwan FDA Registration: d6b302faff71b359c6bbd41bb26f88aa
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Device Details

"Dr. Len" Schuber intraocular lens
TW: โ€œๅšๅฃซๅ€ซโ€่ˆ’ๅšไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3
Cancelled

Registration Details

d6b302faff71b359c6bbd41bb26f88aa

DHA00601834705

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

Oct 01, 2007

Oct 01, 2012

May 05, 2014

Cancellation Information

Logged out

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