Taiwan FDA registration d61a943533f7caa8db4295b1fae3d43a
Waseda Corrective Spectacle Lens (Non-Sterile)
TW: 早稻田 矯正鏡片(未滅菌)
Registration details
- Analysis ID
- d61a943533f7caa8db4295b1fae3d43a
- License Form
- Ministry of Health Medical Device Manufacturing No. 008002
Company information
- Manufacturer
- JP OPTICAL PTE LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Taiwan Waseda Technology 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
- Produced in Taiwan, China; Contract manufacturing
Dates and status
- Registration Date
- Oct 21, 2019
- Expiry Date
- Oct 21, 2024
About this record
Access comprehensive regulatory information for Waseda 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 d61a943533f7caa8db4295b1fae3d43a and manufactured by JP OPTICAL PTE LTD.. The authorized representative in Taiwan is Taiwan Waseda Technology 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.
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