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"Motan" Morgan Eye Surgical Perfusion Device (Unsterilized) - Taiwan Registration e815c36fea168b8ffb47d8cb062662a6

Access comprehensive regulatory information for "Motan" Morgan Eye Surgical Perfusion Device (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e815c36fea168b8ffb47d8cb062662a6 and manufactured by MORTAN, INC.. The authorized representative in Taiwan is OCARE 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.

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e815c36fea168b8ffb47d8cb062662a6
Registration Details
Taiwan FDA Registration: e815c36fea168b8ffb47d8cb062662a6
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Device Details

"Motan" Morgan Eye Surgical Perfusion Device (Unsterilized)
TW: โ€œๆ‘ฉๅฆโ€ๆ‘ฉๆ น็œผ็ง‘ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e815c36fea168b8ffb47d8cb062662a6

DHA04400707000

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 Ophthalmology

M.4360 Perfusion device for ophthalmic surgery

import

Dates and Status

Sep 15, 2008

Sep 15, 2013

Jan 09, 2017

Cancellation Information

Logged out

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