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"SHIE-TUNG" REFRACTOR (Non-Sterile) - Taiwan Registration 531141dbbc3a94ae9ff558c7b078abfa

Access comprehensive regulatory information for "SHIE-TUNG" REFRACTOR (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 531141dbbc3a94ae9ff558c7b078abfa and manufactured by TOWA MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is Synergy Optics 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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531141dbbc3a94ae9ff558c7b078abfa
Registration Details
Taiwan FDA Registration: 531141dbbc3a94ae9ff558c7b078abfa
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Device Details

"SHIE-TUNG" REFRACTOR (Non-Sterile)
TW: "ๅ”ๅŒ" ่‡ช่ฆบๅผ้ฉ—ๅ…‰ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

531141dbbc3a94ae9ff558c7b078abfa

Ministry of Health Medical Device Import No. 015614

DHA09401561400

Company Information

Product Details

M Ophthalmic devices

M1770 Manual Fold Meter

Imported from abroad

Dates and Status

Aug 28, 2015

Aug 28, 2020

Jun 07, 2022

Cancellation Information

Logged out

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