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"Delfi" Pneumatic tourniquet (Non-Sterile) - Taiwan Registration 660aface7676deae676c60e73e9b0911

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 660aface7676deae676c60e73e9b0911 and manufactured by DELFI MEDICAL INNOVATIONS INC.. The authorized representative in Taiwan is MEDEPOT 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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660aface7676deae676c60e73e9b0911
Registration Details
Taiwan FDA Registration: 660aface7676deae676c60e73e9b0911
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Device Details

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

Registration Details

660aface7676deae676c60e73e9b0911

Ministry of Health Medical Device Import No. 018427

DHA09401842703

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

Oct 19, 2017

Oct 19, 2022

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