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"Rheinland" Manual Eye Surgery Instruments (Unsterilized) - Taiwan Registration 662098781e099286f5baa785afbf49ed

Access comprehensive regulatory information for "Rheinland" 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 662098781e099286f5baa785afbf49ed and manufactured by RHEIN MEDICAL INC.. The authorized representative in Taiwan is FEDERAL MEDICAL 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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662098781e099286f5baa785afbf49ed
Registration Details
Taiwan FDA Registration: 662098781e099286f5baa785afbf49ed
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Device Details

"Rheinland" Manual Eye Surgery Instruments (Unsterilized)
TW: "่Š่Œต" ๆ‰‹ๅ‹•ๅผ็œผ็ง‘ๆ‰‹่ก“ๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

662098781e099286f5baa785afbf49ed

DHA04401001206

Company Information

United States

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 14, 2011

Mar 14, 2016

Apr 25, 2018

Cancellation Information

Logged out

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