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“I KEN” Suture Needles (Non-Sterile) - Taiwan Registration 30bcf64c7529c84ab92075700e9866ce

Access comprehensive regulatory information for “I KEN” Suture Needles (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 30bcf64c7529c84ab92075700e9866ce and manufactured by I KEN KOGYO CO., LTD.. The authorized representative in Taiwan is LAIFA 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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30bcf64c7529c84ab92075700e9866ce
Registration Details
Taiwan FDA Registration: 30bcf64c7529c84ab92075700e9866ce
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Device Details

“I KEN” Suture Needles (Non-Sterile)
TW: “醫研”醫療用縫合針 (未滅菌)
Risk Class 1
MD

Registration Details

30bcf64c7529c84ab92075700e9866ce

Ministry of Health Medical Device Import No. 013727

DHA09401372703

Company Information

Japan

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

Dec 26, 2013

Dec 26, 2023