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"Ruida" manual instruments for general surgery (unsterilized) - Taiwan Registration 006c5b31ef86fd43e4e317cdae0ff4f0

Access comprehensive regulatory information for "Ruida" manual instruments for general surgery (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 006c5b31ef86fd43e4e317cdae0ff4f0 and manufactured by REDA INSTRUMENTE GMBH. The authorized representative in Taiwan is Liren Equipment Factory 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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006c5b31ef86fd43e4e317cdae0ff4f0
Registration Details
Taiwan FDA Registration: 006c5b31ef86fd43e4e317cdae0ff4f0
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Device Details

"Ruida" manual instruments for general surgery (unsterilized)
TW: "็‘ž้”"ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

006c5b31ef86fd43e4e317cdae0ff4f0

DHA04400352100

Company Information

Germany

Product Details

It is limited to the scope of first-level identification of medical equipment management measures (manual instruments for general surgery [I.4800]).

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

import

Dates and Status

Apr 12, 2006

Apr 12, 2011

Jan 17, 2013

Cancellation Information

Logged out

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