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"Dr. Len" Ansipine artificial vitreous - Taiwan Registration bbf1ec5b26f40a2337d840e5a7b8503b

Access comprehensive regulatory information for "Dr. Len" Ansipine artificial vitreous in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number bbf1ec5b26f40a2337d840e5a7b8503b and manufactured by LIFECORE BIOMEDICAL, INC.;; BAUSCH & LOMB INCORPORATED. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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bbf1ec5b26f40a2337d840e5a7b8503b
Registration Details
Taiwan FDA Registration: bbf1ec5b26f40a2337d840e5a7b8503b
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Device Details

"Dr. Len" Ansipine artificial vitreous
TW: โ€œๅšๅฃซๅ€ซโ€ๅฎ‰่ฆ–ๅนณไบบๅทฅ็Žป็’ƒ้ซ”
Risk Class 3

Registration Details

bbf1ec5b26f40a2337d840e5a7b8503b

DHA00602510307

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmology

M.4275 ็œผๅ…งๅ……ๅกซ็”จๆถฒ้ซ”

Contract manufacturing;; input

Dates and Status

Jun 01, 2013

Jun 01, 2028