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SILOR Corrective Spectacle Lens (Non-sterile) - Taiwan Registration 16f7f4b8fdffd60f744e59bf1a95e95d

Access comprehensive regulatory information for SILOR 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 16f7f4b8fdffd60f744e59bf1a95e95d and manufactured by ESSILOR-POLYLITE TAIWAN CO., LTD.. The authorized representative in Taiwan is ESSILOR-POLYLITE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ESSILOR MANUFACTURING (THAILAND) CO., LTD., and 1 recent registrations in the same category. 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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16f7f4b8fdffd60f744e59bf1a95e95d
Registration Details
Taiwan FDA Registration: 16f7f4b8fdffd60f744e59bf1a95e95d
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Device Details

SILOR Corrective Spectacle Lens (Non-sterile)
TW: ไพ่ฆ–ๆจ‚ ็Ÿฏๆญฃ้ก็‰‡ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

16f7f4b8fdffd60f744e59bf1a95e95d

Ministry of Health Medical Device Manufacturing No. 006948

Company Information

Taiwan, Province of China

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

Produced in Taiwan, China

Dates and Status

Sep 29, 2017

Sep 29, 2022

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