"Delfi" Pneumatic tourniquet (Non-Sterile)
Taiwan·Risk Class 1·MD·DELFI MEDICAL INNOVATIONS INC.·Registered Jun 23, 2015 – Jun 23, 2025Expired- Analysis ID
- 6bfa75a6302f8c63dbcf20c07aca3e86
- License Form
- Ministry of Health Medical Device Import No. 015370
- Customs Code
- DHA09401537001
- Manufacturer
- DELFI MEDICAL INNOVATIONS INC.
- Manufacturer Country
- Canada
- Authorized Representative
- ZIMMER BIOMET TAIWAN 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
- Jun 23, 2015
- Expiry Date
- Jun 23, 2025
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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 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.