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“RET” Intraocular Lens Guide (Sterile) - Taiwan Registration 1320e36edde9d428a2bda84519d5d171

Access comprehensive regulatory information for “RET” Intraocular Lens Guide (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1320e36edde9d428a2bda84519d5d171 and manufactured by R.E.T., INC.. The authorized representative in Taiwan is BAUSCH & LOMB TAIWAN LIMITED.

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1320e36edde9d428a2bda84519d5d171
Registration Details
Taiwan FDA Registration: 1320e36edde9d428a2bda84519d5d171
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Device Details

“RET” Intraocular Lens Guide (Sterile)
TW: “瑞特” 人工水晶體導引器 (滅菌)
Risk Class 1
MD

Registration Details

1320e36edde9d428a2bda84519d5d171

Ministry of Health Medical Device Import No. 018859

DHA09401885906

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of "Intraocular Lens Guide (M.4300)" under the Measures for the Administration of Medical Equipment.

M Ophthalmic devices

M4300 Intraocular Lens Guide

Imported from abroad

Dates and Status

Mar 05, 2018

Mar 05, 2023