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"Metroton" Eye Surgical Perfusion Device (Unsterilized) - Taiwan Registration 33e25c6d55e390a83ec5dacd433c7485

Access comprehensive regulatory information for "Metroton" 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 33e25c6d55e390a83ec5dacd433c7485 and manufactured by MEDTRONIC XOMED, INC.. The authorized representative in Taiwan is TAIWAN HWA IN ENTERPRISE 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.

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33e25c6d55e390a83ec5dacd433c7485
Registration Details
Taiwan FDA Registration: 33e25c6d55e390a83ec5dacd433c7485
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Device Details

"Metroton" Eye Surgical Perfusion Device (Unsterilized)
TW: โ€œ็พŽ็‰นๅŠ›ๆ•ฆโ€็œผ็›ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

33e25c6d55e390a83ec5dacd433c7485

DHA04400764305

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

Apr 17, 2009

Apr 17, 2014

Nov 15, 2016

Cancellation Information

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