“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.
Device Details
Registration Details
e250c94309b08bc0463525d04dcb2a3d
Ministry of Health Medical Device Import No. 029662
DHA05602966204
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

