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"Delfi" Pneumatic tourniquet (Non-Sterile) - Taiwan Registration 6bfa75a6302f8c63dbcf20c07aca3e86

Access comprehensive regulatory information for "Delfi" 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 6bfa75a6302f8c63dbcf20c07aca3e86 and manufactured by DELFI MEDICAL INNOVATIONS INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DELFI MEDICAL INNOVATIONS INC., and 1 recent registrations in the same category. 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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6bfa75a6302f8c63dbcf20c07aca3e86
Registration Details
Taiwan FDA Registration: 6bfa75a6302f8c63dbcf20c07aca3e86
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Device Details

"Delfi" Pneumatic tourniquet (Non-Sterile)
TW: "ๆˆด็ˆพ่ฒ'ๅ……ๆฐฃๅผๆญข่ก€ๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

6bfa75a6302f8c63dbcf20c07aca3e86

Ministry of Health Medical Device Import No. 015370

DHA09401537001

Company Information

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

Jun 23, 2015

Jun 23, 2025

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