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"Fubi" manual ophthalmic surgical instrument (unsterilized) - Taiwan Registration dd6b3c8180c8ed047a926bf57b88accb

Access comprehensive regulatory information for "Fubi" manual ophthalmic surgical instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd6b3c8180c8ed047a926bf57b88accb and manufactured by PRO-MED INSTRUMENTE GMBH. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, LTD..

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dd6b3c8180c8ed047a926bf57b88accb
Registration Details
Taiwan FDA Registration: dd6b3c8180c8ed047a926bf57b88accb
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Device Details

"Fubi" manual ophthalmic surgical instrument (unsterilized)
TW: "ๆ™ฎ็พŽ" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

dd6b3c8180c8ed047a926bf57b88accb

DHA04400395902

Company Information

Germany

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

Apr 15, 2006

Apr 15, 2011

Jan 18, 2013

Cancellation Information

Logged out

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