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"Dr. Len" Schuber intraocular lens - Taiwan Registration 219ef7f9fa6be4b11381f980878472f3

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 219ef7f9fa6be4b11381f980878472f3 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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219ef7f9fa6be4b11381f980878472f3
Registration Details
Taiwan FDA Registration: 219ef7f9fa6be4b11381f980878472f3
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Device Details

"Dr. Len" Schuber intraocular lens
TW: "ๅšๅฃซๅ€ซ"่ˆ’ๅšไบบๅทฅๆฐดๆ™ถ้ซ”
Risk Class 3

Registration Details

219ef7f9fa6be4b11381f980878472f3

DHA00601696202

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

Aug 04, 2006

Aug 04, 2026

Companies Making Similar Products
Top companies providing products similar to ""Dr. Len" Schuber intraocular lens"

BAUSCH & LOMB INC.

1 products

Latest registration: Oct 01, 2007

Recent Registrations
Recently registered similar products

"Dr. Len" Schuber intraocular lens

Oct 01, 2007
Manufacturer:

BAUSCH & LOMB INC.

Registration:

d6b302faff71b359c6bbd41bb26f88aa

Risk Class:

3