Taiwan FDA registration 7c4488de7388a6791841796308505b52

"PARIS MIKI OPTICAL" Corrective spectacle lens (Non-Sterile)

TW: "巴黎三城眼鏡" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·AICHI-NIKON·Registered Apr 15, 2016 – Apr 15, 2021Expired
Registration details
Analysis ID
7c4488de7388a6791841796308505b52
License Form
Ministry of Health Medical Device Import No. 016401
Customs Code
DHA09401640101
Company information
Manufacturer
AICHI-NIKON
Manufacturer Country
Japan
Authorized Representative
PARIS MIKI OPTICAL 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
Apr 15, 2016
Expiry Date
Apr 15, 2021
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About this record

Access comprehensive regulatory information for "PARIS MIKI OPTICAL" 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 7c4488de7388a6791841796308505b52 and manufactured by AICHI-NIKON. The authorized representative in Taiwan is PARIS MIKI OPTICAL TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including CENTROSTYLE S.P.A., EHS LENS PHILIPPINES, INC., and 5 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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