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Medtronic Manual Eye Surgery Instruments (Unsterilized) - Taiwan Registration 50325a239f1336c781e5379c6bccf39e

Access comprehensive regulatory information for Medtronic Manual Eye Surgery Instruments (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 50325a239f1336c781e5379c6bccf39e and manufactured by MEDTRONIC XOMED INSTRUMENTATION SAS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MEDTRONIC XOMED, INC., and 1 recent registrations in the same category. 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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50325a239f1336c781e5379c6bccf39e
Registration Details
Taiwan FDA Registration: 50325a239f1336c781e5379c6bccf39e
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Device Details

Medtronic Manual Eye Surgery Instruments (Unsterilized)
TW: โ€œ็พŽๆ•ฆๅŠ›โ€ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ๏ผˆๆœชๆป…่Œ๏ผ‰
Risk Class 1
Cancelled

Registration Details

50325a239f1336c781e5379c6bccf39e

DHA04400864807

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Eye Surgery Instruments (M.4350)".

M Ophthalmology

M.4350 ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ

import

Dates and Status

Mar 26, 2010

Mar 26, 2015

Apr 25, 2018

Cancellation Information

Logged out

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