Taiwan FDA registration a0210fda1276676b7fd24799b53c836c

"HOYA" Corrective spectacle lens (Non-Sterile)

TW: "豪雅" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.·Registered Mar 19, 2020 – Mar 19, 2025Expired
Registration details
Analysis ID
a0210fda1276676b7fd24799b53c836c
License Form
Ministry of Health Medical Device Land Transport No. 004116
Customs Code
DHA09600411602
Company information
Manufacturer Country
China
Authorized Representative
HOYA LENS TAIWAN 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; Made in China
Dates and status
Registration Date
Mar 19, 2020
Expiry Date
Mar 19, 2025
Companies making similar products

Top companies providing products similar to ""HOYA" Corrective spectacle lens (Non-Sterile)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "HOYA" 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 a0210fda1276676b7fd24799b53c836c and manufactured by DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.. The authorized representative in Taiwan is HOYA LENS TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION, and 1 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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations