Taiwan FDA registration 65f80b8b860e6b32b4ba457bbd1d360a

"DAEMYUNG" SHINOBI Corrective Spectacle Lens (Non-Sterile)

TW: "台灣大明" 矯正鏡片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·DAEMYUNG OPTICAL CO., LTD·Registered Mar 22, 2016 – Mar 22, 2021Expired
Registration details
Analysis ID
65f80b8b860e6b32b4ba457bbd1d360a
License Form
Ministry of Health Medical Device Import No. 016292
Customs Code
DHA09401629209
Company information
Manufacturer Country
Korea, Republic of
Authorized Representative
TAIWAN TAMING OPTICAL 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
Mar 22, 2016
Expiry Date
Mar 22, 2021
About this record

Access comprehensive regulatory information for "DAEMYUNG" SHINOBI 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 65f80b8b860e6b32b4ba457bbd1d360a and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is TAIWAN TAMING OPTICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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+ Devices