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"Delfi" Pneumatic tourniquet(Non-sterile) - Taiwan Registration b07425b2e9880ccc6e2661a2d23eb093

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 b07425b2e9880ccc6e2661a2d23eb093 and manufactured by DELFI MEDICAL INNOVATIONS INC.. The authorized representative in Taiwan is Jia Di 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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b07425b2e9880ccc6e2661a2d23eb093
Registration Details
Taiwan FDA Registration: b07425b2e9880ccc6e2661a2d23eb093
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Device Details

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

Registration Details

b07425b2e9880ccc6e2661a2d23eb093

Ministry of Health Medical Device Import No. 022140

DHA09402214001

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

Nov 30, 2020

Nov 30, 2025