Taiwan FDA registration 219ef7f9fa6be4b11381f980878472f3

"Dr. Len" Schuber intraocular lens

TW: "博士倫"舒博人工水晶體
Taiwan flagTaiwan·Risk Class 3·BAUSCH & LOMB INC.·Registered Aug 04, 2006 – Aug 04, 2026Active
Registration details
Analysis ID
219ef7f9fa6be4b11381f980878472f3
Customs Code
DHA00601696202
Company information
Manufacturer
BAUSCH & LOMB INC.
Manufacturer Country
United States
Authorized Representative
BAUSCH & LOMB TAIWAN LIMITED
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.3600 Artificial Crystal
Import Information
import
Dates and status
Registration Date
Aug 04, 2006
Expiry Date
Aug 04, 2026
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About this record

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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