Taiwan FDA registration 95c391ccaa536db5b23d9b692b876238

"Dexing" pressurized tourniquet (unsterilized)

TW: “德興”加壓止血帶 (未滅菌)

Taiwan·Risk Class 1·DE XING MEDICAL TREATMENT AND INSTRUMENT CO., LTD.·Registered Jan 07, 2020 – Jan 07, 2030Active

Registration details

Analysis ID: 95c391ccaa536db5b23d9b692b876238

Company information

Manufacturer: DE XING MEDICAL TREATMENT AND INSTRUMENT CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: DE XING MEDICAL TREATMENT AND INSTRUMENT 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: Domestic

Dates and status

Registration Date: Jan 07, 2020
Expiry Date: Jan 07, 2030

About this record

Access comprehensive regulatory information for "Dexing" pressurized tourniquet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 95c391ccaa536db5b23d9b692b876238 and manufactured by DE XING MEDICAL TREATMENT AND INSTRUMENT CO., LTD.. The authorized representative in Taiwan is DE XING MEDICAL TREATMENT AND INSTRUMENT CO., LTD..

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