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Rheinland Manual Eye Surgery Instruments (Sterilization) - Taiwan Registration 09b5a6d3c095ec84ff31e590c89b9727

Access comprehensive regulatory information for Rheinland Manual Eye Surgery Instruments (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 09b5a6d3c095ec84ff31e590c89b9727 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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09b5a6d3c095ec84ff31e590c89b9727
Registration Details
Taiwan FDA Registration: 09b5a6d3c095ec84ff31e590c89b9727
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Device Details

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

Registration Details

09b5a6d3c095ec84ff31e590c89b9727

DHA04401079907

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

Input;; QMS/QSD

Dates and Status

Sep 02, 2011

Sep 02, 2016

Apr 25, 2018

Cancellation Information

Logged out

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