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"Keeler" Magnification Loupes and accessories (Non-Sterile) - Taiwan Registration 26e1d2c64f91a01795a0cf41a805615d

Access comprehensive regulatory information for "Keeler" Magnification Loupes and accessories (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 26e1d2c64f91a01795a0cf41a805615d and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Keeler Limited, 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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26e1d2c64f91a01795a0cf41a805615d
Registration Details
Taiwan FDA Registration: 26e1d2c64f91a01795a0cf41a805615d
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Device Details

"Keeler" Magnification Loupes and accessories (Non-Sterile)
TW: "ๅฅ‡ๅ‹’"ๆ‰‹่ก“ๆ”พๅคง้กๅŠๅ…ถ้™„ไปถ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

26e1d2c64f91a01795a0cf41a805615d

Ministry of Health Medical Device Import No. 014884

DHA09401488401

Company Information

United Kingdom

Product Details

M Ophthalmic devices

M4770 Ophthalmic surgical glasses (magnifying glasses)

Imported from abroad

Dates and Status

Jan 29, 2015

Jan 29, 2025

Cancellation Information

Logged out

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