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"DS Maref" Pneumatic tourniquet (Non-Sterile) - Taiwan Registration 78f7f6e21cd617084540a50e90cf387c

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..

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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78f7f6e21cd617084540a50e90cf387c
Registration Details
Taiwan FDA Registration: 78f7f6e21cd617084540a50e90cf387c
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Device Details

"DS Maref" Pneumatic tourniquet (Non-Sterile)
TW: "่ฟชๆ–ฏ็‘ช้‡Œๅคซ" ๅ……ๆฐฃๅผๆญข่ก€ๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

78f7f6e21cd617084540a50e90cf387c

Ministry of Health Medical Device Import No. 016541

DHA09401654104

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Inflatable Tourniquet (I.5910)".

I General and plastic surgical devices

I5910 Inflatable tourniquet

Imported from abroad

Dates and Status

May 16, 2016

May 16, 2026