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"Medica" eye surgical perfusion device (unsterilized) - Taiwan Registration ab330a4642187fce02a2982981d552b5

Access comprehensive regulatory information for "Medica" 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 ab330a4642187fce02a2982981d552b5 and manufactured by MEDICEL AT. The authorized representative in Taiwan is RAY HUNG 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.

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ab330a4642187fce02a2982981d552b5
Registration Details
Taiwan FDA Registration: ab330a4642187fce02a2982981d552b5
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Device Details

"Medica" eye surgical perfusion device (unsterilized)
TW: "็พŽ่ฟชๅก"็œผ็›ๆ‰‹่ก“็Œๆณจ่ฃ็ฝฎ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

ab330a4642187fce02a2982981d552b5

DHA04401076809

Company Information

Switzerland

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

Aug 29, 2011

Aug 29, 2016

Jun 28, 2018

Cancellation Information

Logged out

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