Taiwan FDA registration aaeff898dc19cb90c9e7d7eaebb94a1a

DIAMOND Corrective Spectacle Lens (Non-Sterile)

TW: 晶鑽矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·HONG KONG OPTICAL LENS CO., LTD.·Registered May 30, 2019 – May 30, 2024Expired

Registration details

Analysis ID: aaeff898dc19cb90c9e7d7eaebb94a1a
License Form: Ministry of Health Medical Device Import No. 020505
Customs Code: DHA09402050502

Company information

Manufacturer: HONG KONG OPTICAL LENS CO., LTD.
Manufacturer Country: Hong Kong
Authorized Representative: HKO OPTICAL LENS (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: May 30, 2019
Expiry Date: May 30, 2024

About this record

Access comprehensive regulatory information for DIAMOND 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 aaeff898dc19cb90c9e7d7eaebb94a1a and manufactured by HONG KONG OPTICAL LENS CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

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