Pure Global

"Mortan" Ocular Surgery Irrigation Device (Non-Sterile) - Taiwan Registration a9f2b439d581003d2bfeb62097e30d76

Access comprehensive regulatory information for "Mortan" Ocular Surgery Irrigation Device (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 a9f2b439d581003d2bfeb62097e30d76 and manufactured by MORTAN, INC.. The authorized representative in Taiwan is BIOMEGA 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
a9f2b439d581003d2bfeb62097e30d76
Registration Details
Taiwan FDA Registration: a9f2b439d581003d2bfeb62097e30d76
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Mortan" Ocular Surgery Irrigation Device (Non-Sterile)
TW: "ๆ‘ฉ้ “" ็œผ็ง‘ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

a9f2b439d581003d2bfeb62097e30d76

Ministry of Health Medical Device Import No. 017211

DHA09401721101

Company Information

United States

Product Details

Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Eye Surgical Perfusion Device (M.4360)".

M Ophthalmic devices

M4360 Surgical perfusion device for the eye

Imported from abroad

Dates and Status

Nov 25, 2016

Nov 25, 2021