Pure Global

"Lominnis" WiseVision laser indirect fundus lens - Taiwan Registration 3558a74c01ca16ae1ce7323821766614

Access comprehensive regulatory information for "Lominnis" WiseVision laser indirect fundus lens in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3558a74c01ca16ae1ce7323821766614 and manufactured by Lumenis Be Inc.;; KEELER LTD.. The authorized representative in Taiwan is (Hong Kong) Lumenis Be (HK) Limited, Taiwan Branch.

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
3558a74c01ca16ae1ce7323821766614
Registration Details
Taiwan FDA Registration: 3558a74c01ca16ae1ce7323821766614
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Lominnis" WiseVision laser indirect fundus lens
TW: โ€œๆด›ๆ˜Žๅฐผๆ–ฏโ€ๆ…ง่ฆ–้›ทๅฐ„้–“ๆŽฅ็œผๅบ•้ก
Risk Class 2

Registration Details

3558a74c01ca16ae1ce7323821766614

DHA05603278300

Company Information

United Kingdom;;United States

Product Details

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

M Ophthalmology

M.1570 Fundus Mirrors

Contract manufacturing;; input

Dates and Status

Aug 08, 2019

Aug 08, 2029