Taiwan FDA registration dd1cf9e7bbadd8cf6d1e7fd2a0ef4459

“LICAR” Corrective Spectacle Lens (Non-Sterile)

TW: "生茂"矯正鏡片(未滅菌)

Taiwan·Risk Class 1·MD·DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.·Registered Mar 08, 2021 – Mar 08, 2026Expired

Registration details

Analysis ID: dd1cf9e7bbadd8cf6d1e7fd2a0ef4459
License Form: Ministry of Health Medical Device Land Transport No. 004459
Customs Code: DHA09600445906

Company information

Manufacturer: DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.
Manufacturer Country: China
Authorized Representative: SHENG MAO 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; Made in China

Dates and status

Registration Date: Mar 08, 2021
Expiry Date: Mar 08, 2026

About this record

Access comprehensive regulatory information for “LICAR” 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 dd1cf9e7bbadd8cf6d1e7fd2a0ef4459 and manufactured by DAEJEON DAEMYUNG OPTICAL (HANGZHOU) CO.,LTD.. The authorized representative in Taiwan is SHENG MAO 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.