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“Keeler” Indirect Ophthalmoscope and Accessories - Taiwan Registration 626cd7d39f823595b11048231b10c7b4

Access comprehensive regulatory information for “Keeler” Indirect Ophthalmoscope and Accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 626cd7d39f823595b11048231b10c7b4 and manufactured by Keeler Limited. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., LTD..

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626cd7d39f823595b11048231b10c7b4
Registration Details
Taiwan FDA Registration: 626cd7d39f823595b11048231b10c7b4
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Device Details

“Keeler” Indirect Ophthalmoscope and Accessories
TW: “奇勒” 間接眼底鏡及其附件
Risk Class 2
MD

Registration Details

626cd7d39f823595b11048231b10c7b4

Ministry of Health Medical Device Import No. 025572

DHA05602557209

Company Information

United Kingdom

Product Details

For details, it is Chinese approved copy of the imitation order

M Ophthalmic devices

M1570 fundus mirror

Imported from abroad

Dates and Status

Oct 31, 2013

Oct 31, 2028