Taiwan FDA registration ff320dcac6f82f4abbd159d11af38376

"Medico" single-point pressurized hemostatic device (unsterilized)

TW: “美迪克” 單點加壓式止血器(未滅菌)

Taiwan·Risk Class 1·TOGO MEDIKIT CO., LTD. HYUGA FACTORY·Registered Dec 03, 2021 – Dec 03, 2026Active

Registration details

Analysis ID: ff320dcac6f82f4abbd159d11af38376
Customs Code: DHA09402271102

Company information

Manufacturer: TOGO MEDIKIT CO., LTD. HYUGA FACTORY
Manufacturer Country: Japan
Authorized Representative: BIOMEDIWORLD HEALTHCARE CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the "non-inflatable tourniquet (I.5900)" of the Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.5900 非充氣式止血帶
Import Information: import

Dates and status

Registration Date: Dec 03, 2021
Expiry Date: Dec 03, 2026

About this record

Access comprehensive regulatory information for "Medico" single-point pressurized hemostatic device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ff320dcac6f82f4abbd159d11af38376 and manufactured by TOGO MEDIKIT CO., LTD. HYUGA FACTORY. The authorized representative in Taiwan is BIOMEDIWORLD HEALTHCARE CO., LTD..

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