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"Integra" Jarit Manual surgical instrument for general use (Non-Sterile) - Taiwan Registration d48384d39504c3f6c787fcd95e800668

Access comprehensive regulatory information for "Integra" Jarit 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 d48384d39504c3f6c787fcd95e800668 and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is KINDMED CORPORATION.

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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d48384d39504c3f6c787fcd95e800668
Registration Details
Taiwan FDA Registration: d48384d39504c3f6c787fcd95e800668
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Device Details

"Integra" Jarit Manual surgical instrument for general use (Non-Sterile)
TW: "ๆฎท็‰นๆญŒ็ˆพ" ๆฝ”็‘žไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

d48384d39504c3f6c787fcd95e800668

Ministry of Health Medical Device Import No. 016281

DHA09401628104

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Mar 21, 2016

Mar 21, 2021