Pure Global

"Kaile" fundus lens series and accessories - Taiwan Registration 1e5a71c1e67004a931fab0eff565024a

Access comprehensive regulatory information for "Kaile" fundus lens series 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 1e5a71c1e67004a931fab0eff565024a and manufactured by KEELER LTD.. The authorized representative in Taiwan is TAIWAN OPTICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
1e5a71c1e67004a931fab0eff565024a
Registration Details
Taiwan FDA Registration: 1e5a71c1e67004a931fab0eff565024a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Kaile" fundus lens series and accessories
TW: "ๅ‡ฑๆจ‚"็œผๅบ•้ก็ณปๅˆ—ๅŠ้™„ไปถ
Risk Class 2

Registration Details

1e5a71c1e67004a931fab0eff565024a

DHA00601668400

Company Information

United Kingdom

Product Details

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

M Ophthalmology

import

Dates and Status

Jun 14, 2006

Jun 14, 2026