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“BEBRE” Vision Corrective Spectacle Lens(Non-sterile) - Taiwan Registration 0c7590f1febd0210ce282f4286963161

Access comprehensive regulatory information for “BEBRE” Vision Corrective Spectacle Lens(Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 0c7590f1febd0210ce282f4286963161 and manufactured by ESSILOR MANUFACTURING (THAILAND) CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

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0c7590f1febd0210ce282f4286963161
Registration Details
Taiwan FDA Registration: 0c7590f1febd0210ce282f4286963161
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Device Details

“BEBRE” Vision Corrective Spectacle Lens(Non-sterile)
TW: “倍視樂” 視光矯正鏡片 (未滅菌)
Risk Class 1
MD

Registration Details

0c7590f1febd0210ce282f4286963161

Ministry of Health Medical Device Import No. 019554

DHA09401955402

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Aug 30, 2018

Aug 30, 2028