Taiwan FDA registration 0c7590f1febd0210ce282f4286963161

“BEBRE” Vision Corrective Spectacle Lens(Non-sterile)

TW: “倍視樂” 視光矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·ESSILOR MANUFACTURING (THAILAND) CO., LTD.·Registered Aug 30, 2018 – Aug 30, 2028Active

Registration details

Analysis ID: 0c7590f1febd0210ce282f4286963161
License Form: Ministry of Health Medical Device Import No. 019554
Customs Code: DHA09401955402

Company information

Manufacturer: ESSILOR MANUFACTURING (THAILAND) CO., LTD.
Manufacturer Country: Thailand
Authorized Representative: ESSILOR-POLYLITE TAIWAN CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".
Product Type (Level 1): M Ophthalmic devices
Product Type (Level 2): M5844 corrective lenses
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 30, 2018
Expiry Date: Aug 30, 2028

About this record

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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