Taiwan FDA registration 539958b80fcbebb67b81ce0accdba9b2

MONODESIGN lens corrective spectacle lens (Non-sterile)　

TW: “聯全”矯正鏡片 (未滅菌)

Taiwan·Risk Class 1·MD·FUJITA OPTICAL CO., LTD.·Registered Feb 18, 2014 – Feb 18, 2024Expired

Registration details

Analysis ID: 539958b80fcbebb67b81ce0accdba9b2
License Form: Ministry of Health Medical Device Import No. 013856
Customs Code: DHA09401385601

Company information

Manufacturer: FUJITA OPTICAL CO., LTD.
Manufacturer Country: Japan
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: Feb 18, 2014
Expiry Date: Feb 18, 2024

About this record

Access comprehensive regulatory information for MONODESIGN lens 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 539958b80fcbebb67b81ce0accdba9b2 and manufactured by FUJITA OPTICAL CO., LTD.. The authorized representative in Taiwan is HKO OPTICAL LENS (TAIWAN) CO., LTD..

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