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"Integra" Jarit instrument case (Non-Sterile) - Taiwan Registration e767351b546543470843f7b63e929b2a

Access comprehensive regulatory information for "Integra" Jarit instrument case (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 e767351b546543470843f7b63e929b2a and manufactured by BAHADIR CORPORATION. The authorized representative in Taiwan is KINDMED CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including INTEGRA YORK PA, INC., and 1 recent registrations in the same category. 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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e767351b546543470843f7b63e929b2a
Registration Details
Taiwan FDA Registration: e767351b546543470843f7b63e929b2a
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Device Details

"Integra" Jarit instrument case (Non-Sterile)
TW: "ๆฎท็‰นๆญŒ็ˆพ" ๆฝ”็‘žๅ™จๆขฐ็›’ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e767351b546543470843f7b63e929b2a

Ministry of Health Medical Device Import No. 018027

DHA09401802700

Company Information

Turkey

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

Jun 30, 2017

Jun 30, 2022

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