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SOLOMAX Corrective Spectacle Lens (Non-Sterile) - Taiwan Registration 2f59394ad69a8870f14b2ca713d1898e

Access comprehensive regulatory information for SOLOMAX 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 2f59394ad69a8870f14b2ca713d1898e and manufactured by ASAHI LITE OPTICAL CO., LTD.. The authorized representative in Taiwan is SUNRISE 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.

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2f59394ad69a8870f14b2ca713d1898e
Registration Details
Taiwan FDA Registration: 2f59394ad69a8870f14b2ca713d1898e
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Device Details

SOLOMAX Corrective Spectacle Lens (Non-Sterile)
TW: ๅฃซๆจ‚ๆ‘ฉ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2f59394ad69a8870f14b2ca713d1898e

Ministry of Health Medical Device Import No. 020811

DHA09402081109

Company Information

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Corrective Lenses (M.5844)".

M Ophthalmic devices

M5844 corrective lenses

Imported from abroad

Dates and Status

Sep 02, 2019

Sep 02, 2024