Pure Global

"Translite" Transilluminator (Non-Sterile) - Taiwan Registration a34f4aa6552019df95f82de6d985affc

Access comprehensive regulatory information for "Translite" Transilluminator (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a34f4aa6552019df95f82de6d985affc and manufactured by TRANSLITE LLC. The authorized representative in Taiwan is ADENT MED 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
a34f4aa6552019df95f82de6d985affc
Registration Details
Taiwan FDA Registration: a34f4aa6552019df95f82de6d985affc
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Translite" Transilluminator (Non-Sterile)
TW: "็ฉฟ่ฆ–ไพ†้€"้€็…งๅ™จ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

a34f4aa6552019df95f82de6d985affc

Ministry of Health Medical Device Import No. 015964

DHA09401596401

Company Information

United States

Product Details

M Ophthalmic devices

M1945 transillumination

Imported from abroad

Dates and Status

Dec 11, 2015

Dec 11, 2020

Aug 05, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€