Taiwan FDA registration bf43bab4616f52b5a6e0f21439e44b8a

"Bausch & Len" Ansie can be artificial vitreous

TW: "博士倫" 安視可人工玻璃體
Taiwan flagTaiwan·MANUFACTURED BY ANIKA THERAPEUTICS, INC. FOR BAUSCH & LOMB INC.·Registered Jan 14, 2005 – Jan 14, 2010Cancelled
Registration details
Analysis ID
bf43bab4616f52b5a6e0f21439e44b8a
Customs Code
DHA00601101204
Company information
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
Jan 14, 2005
Expiry Date
Jan 14, 2010
Cancellation Date
Jun 30, 2010
Cancellation information
Status
Logged out
Reason
自請註銷
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About this record

Access comprehensive regulatory information for "Bausch & Len" Ansie can be artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. is registered under number bf43bab4616f52b5a6e0f21439e44b8a and manufactured by MANUFACTURED BY ANIKA THERAPEUTICS, INC. FOR 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 LIFECORE BIOMEDICAL, INC.;; BAUSCH & LOMB INCORPORATED, 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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