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"Keeler" Magnification Loupes and accessories (Non-Sterile) - Taiwan Registration 83c54b82ddc93a36e7c17ca1947375fc

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 83c54b82ddc93a36e7c17ca1947375fc 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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83c54b82ddc93a36e7c17ca1947375fc
Registration Details
Taiwan FDA Registration: 83c54b82ddc93a36e7c17ca1947375fc
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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

Registration Details

83c54b82ddc93a36e7c17ca1947375fc

Ministry of Health Medical Device Import Registration No. 014884

DHA08401488402

Company Information

United Kingdom

Product Details

Limited to the first level of identification scope of "Ophthalmic Surgical Glasses (Magnifying Glasses) (M.4770)" under the Measures for the Administration of Medical Devices.

M Ophthalmic devices

M4770 Ophthalmic surgical glasses (magnifying glasses)

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2025

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