Taiwan FDA registration 47857bb98c0a6d0e8ec09f1ee1eaccc4

"Bausch & Len" IOL Guide (Sterilization)

TW: "博士倫" 人工水晶體導引器 (滅菌)
Taiwan flagTaiwan·Risk Class 1·BAUSCH & LOMB INC.·Registered Apr 13, 2006 – Apr 13, 2026Expired
Registration details
Analysis ID
47857bb98c0a6d0e8ec09f1ee1eaccc4
Customs Code
DHA04400372105
Company information
Manufacturer
BAUSCH & LOMB INC.
Manufacturer Country
United States
Authorized Representative
BAUSCH & LOMB TAIWAN LIMITED
Product details
Intended Use
Limited to the first level identification range of "intraocular lens guide (M.4300)" of the Classification and Grading Management Measures for Medical Equipment.
Product Type (Level 1)
M Ophthalmology
Product Type (Level 2)
M.4300 Artificial crystal body inducer
Import Information
import
Dates and status
Registration Date
Apr 13, 2006
Expiry Date
Apr 13, 2026
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About this record

Access comprehensive regulatory information for "Bausch & Len" IOL Guide (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 47857bb98c0a6d0e8ec09f1ee1eaccc4 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, 2 companies making similar products including BAUSCH & LOMB INC., MEDICEL AT, and 2 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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