Taiwan FDA registration ee0c6f92c7398e114e87943b2ad70c41

"TA FA" Nonpneumatic Tourniquet (Non-Sterile)

TW: "大發" 非充氣式止血帶 (未滅菌)

Taiwan·Risk Class 1·MD·MUNETA GOMU CO., LTD.·Registered Dec 16, 2013 – Dec 16, 2023Expired

Registration details

Analysis ID: ee0c6f92c7398e114e87943b2ad70c41
License Form: Ministry of Health Medical Device Import No. 013681
Customs Code: DHA09401368105

Company information

Manufacturer: MUNETA GOMU CO., LTD.
Manufacturer Country: Japan
Authorized Representative: LAIFA CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Non-inflatable Tourniquet (I.5900)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I5900 Non-inflatable tourniquet
Import Information: Imported from abroad

Dates and status

Registration Date: Dec 16, 2013
Expiry Date: Dec 16, 2023

About this record

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.