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“Keeler” Direct Ophthalmoscope - Taiwan Registration e250c94309b08bc0463525d04dcb2a3d

Access comprehensive regulatory information for “Keeler” Direct Ophthalmoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e250c94309b08bc0463525d04dcb2a3d and manufactured by KEELER LTD.. The authorized representative in Taiwan is EVERLIGHT INSTRUMENT CO., 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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e250c94309b08bc0463525d04dcb2a3d
Registration Details
Taiwan FDA Registration: e250c94309b08bc0463525d04dcb2a3d
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Device Details

“Keeler” Direct Ophthalmoscope
TW: “奇勒”直接眼底鏡
Risk Class 2
MD

Registration Details

e250c94309b08bc0463525d04dcb2a3d

Ministry of Health Medical Device Import No. 029662

DHA05602966204

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

Apr 18, 2017

Apr 18, 2027