Taiwan FDA registration 78f7f6e21cd617084540a50e90cf387c

"DS Maref" Pneumatic tourniquet (Non-Sterile)

TW: "迪斯瑪里夫" 充氣式止血帶 (未滅菌)

Taiwan·Risk Class 1·MD·DAESUNG MAREF CO., LTD.·Registered May 16, 2016 – May 16, 2026Expired

Registration details

Analysis ID: 78f7f6e21cd617084540a50e90cf387c
License Form: Ministry of Health Medical Device Import No. 016541
Customs Code: DHA09401654104

Company information

Manufacturer: DAESUNG MAREF CO., LTD.
Manufacturer Country: Korea, Republic of
Authorized Representative: HONG YU MEDICAL CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I5910 Inflatable tourniquet
Import Information: Imported from abroad

Dates and status

Registration Date: May 16, 2016
Expiry Date: May 16, 2026

About this record

Access comprehensive regulatory information for "DS Maref" Pneumatic 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 78f7f6e21cd617084540a50e90cf387c and manufactured by DAESUNG MAREF CO., LTD.. The authorized representative in Taiwan is HONG YU MEDICAL CO., LTD..

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