"Delfi" Pneumatic tourniquet (Non-Sterile)
Taiwan·Risk Class 1·MD·DELFI MEDICAL INNOVATIONS INC.·Registered Oct 19, 2017 – Oct 19, 2022Expired- Analysis ID
- 660aface7676deae676c60e73e9b0911
- License Form
- Ministry of Health Medical Device Import No. 018427
- Customs Code
- DHA09401842703
- Manufacturer
- DELFI MEDICAL INNOVATIONS INC.
- Manufacturer Country
- Canada
- Authorized Representative
- MEDEPOT CO., LTD
- 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
- Registration Date
- Oct 19, 2017
- Expiry Date
- Oct 19, 2022
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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.