Pure Global

“Keeler” Cryophthalmic unit and accessories - Taiwan Registration 8b718fccf74705557f07b462dbd5bc5a

Access comprehensive regulatory information for “Keeler” Cryophthalmic unit 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 8b718fccf74705557f07b462dbd5bc5a and manufactured by Keeler Limited. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
8b718fccf74705557f07b462dbd5bc5a
Registration Details
Taiwan FDA Registration: 8b718fccf74705557f07b462dbd5bc5a
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Keeler” Cryophthalmic unit and accessories
TW: “奇勒”眼科冷凍儀及其附件
Risk Class 2
MD

Registration Details

8b718fccf74705557f07b462dbd5bc5a

Ministry of Health Medical Device Import No. 025312

DHA05602531209

Company Information

United Kingdom

Product Details

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

M Ophthalmic devices

M4170 Eye Cryometer

Imported from abroad

Dates and Status

Jul 31, 2013

Jul 31, 2028