Taiwan FDA registration ddd53bf536df14ac04253dd30bd8aea8
"DAEMYUNG" Optical Corrective Spectacle Lens (Non-Sterile)
TW: "大明" 光學矯正鏡片 (未滅菌)
Registration details
- Analysis ID
- ddd53bf536df14ac04253dd30bd8aea8
- License Form
- Ministry of Health Medical Device Import No. 018110
- Customs Code
- DHA09401811000
Company information
- Manufacturer
- DAEMYUNG OPTICAL CO., LTD
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- YI JIA YI 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
- Jul 26, 2017
- Expiry Date
- Jul 26, 2022
About this record
Access comprehensive regulatory information for "DAEMYUNG" 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 ddd53bf536df14ac04253dd30bd8aea8 and manufactured by DAEMYUNG OPTICAL CO., LTD. The authorized representative in Taiwan is YI JIA YI 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