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"INVIDIA" Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration ca4387656afd0b1a2ed7e2f1fd4b3627

Access comprehensive regulatory information for "INVIDIA" Manual surgical instrument for general use (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ca4387656afd0b1a2ed7e2f1fd4b3627 and manufactured by INVIDIA MEDICAL GMBH & CO. KG. The authorized representative in Taiwan is JINXIANG TECHNOLOGY CO., LTD..

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ca4387656afd0b1a2ed7e2f1fd4b3627
Registration Details
Taiwan FDA Registration: ca4387656afd0b1a2ed7e2f1fd4b3627
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Device Details

"INVIDIA" Manual surgical instrument for general use (Non-Sterile)
TW: "้Šฆๅพฎๅพท้›…" ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

ca4387656afd0b1a2ed7e2f1fd4b3627

Ministry of Health Medical Device Import No. 015080

DHA09401508002

Company Information

Product Details

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 07, 2015

Apr 07, 2020

Jun 22, 2022

Cancellation Information

Logged out

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