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"Ashi" Manual Eye Surgery Instruments (Unsterilized) - Taiwan Registration d1bf4cf28c73966b3fc4ebb810cc82cc

Access comprehensive regulatory information for "Ashi" 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 d1bf4cf28c73966b3fc4ebb810cc82cc and manufactured by RZ MEDIZINTECHNIK GMBH. The authorized representative in Taiwan is Shanghua Industrial 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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d1bf4cf28c73966b3fc4ebb810cc82cc
Registration Details
Taiwan FDA Registration: d1bf4cf28c73966b3fc4ebb810cc82cc
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Device Details

"Ashi" Manual Eye Surgery Instruments (Unsterilized)
TW: โ€œ้›…่ฆ–โ€ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

d1bf4cf28c73966b3fc4ebb810cc82cc

DHA04400774908

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

May 22, 2009

May 22, 2014

Dec 14, 2016

Cancellation Information

Logged out

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