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"TA FA" Nonpneumatic Tourniquet (Non-Sterile) - Taiwan Registration ee0c6f92c7398e114e87943b2ad70c41

Access comprehensive regulatory information for "TA FA" Nonpneumatic Tourniquet (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 ee0c6f92c7398e114e87943b2ad70c41 and manufactured by MUNETA GOMU 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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ee0c6f92c7398e114e87943b2ad70c41
Registration Details
Taiwan FDA Registration: ee0c6f92c7398e114e87943b2ad70c41
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Device Details

"TA FA" Nonpneumatic Tourniquet (Non-Sterile)
TW: "ๅคง็™ผ" ้žๅ……ๆฐฃๅผๆญข่ก€ๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ee0c6f92c7398e114e87943b2ad70c41

Ministry of Health Medical Device Import No. 013681

DHA09401368105

Company Information

Japan

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".

I General and plastic surgical devices

I5900 Non-inflatable tourniquet

Imported from abroad

Dates and Status

Dec 16, 2013

Dec 16, 2023