Handes Corrective Spectacle Lens (Non-Sterile)
Taiwan·Risk Class 1·MD·Tainan Factory of Taiwan Branch of Singapore Shangtiange Technology Co., Ltd·Registered Sep 22, 2021 – Sep 22, 2026Active- Analysis ID
- 69b24f62a5261bc5ecb96a42c3f3a908
- License Form
- Ministry of Health Medical Device Manufacturing No. 009320
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TGT HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE)
- Intended Use
- Limited to the first level identification scope of the "corrective lenses (M.5844)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- M Ophthalmic devices
- Product Type (Level 2)
- M5844 corrective lenses
- Import Information
- Produced in Taiwan, China
- Registration Date
- Sep 22, 2021
- Expiry Date
- Sep 22, 2026
Access comprehensive regulatory information for Handes 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 69b24f62a5261bc5ecb96a42c3f3a908 and manufactured by Tainan Factory of Taiwan Branch of Singapore Shangtiange Technology Co., Ltd. The authorized representative in Taiwan is TGT HOLDINGS PTE. LTD. TAIWAN BRANCH (SINGAPORE).
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.