Taiwan FDA registration b07425b2e9880ccc6e2661a2d23eb093

"Delfi" Pneumatic tourniquet(Non-sterile)

TW: "岱爾菲" 充氣式止血帶(未滅菌)

Taiwan·Risk Class 1·MD·DELFI MEDICAL INNOVATIONS INC.·Registered Nov 30, 2020 – Nov 30, 2025Expired

Registration details

Analysis ID: b07425b2e9880ccc6e2661a2d23eb093
License Form: Ministry of Health Medical Device Import No. 022140
Customs Code: DHA09402214001

Company information

Manufacturer: DELFI MEDICAL INNOVATIONS INC.
Manufacturer Country: Canada
Authorized Representative: Jia Di Medical co., ltd.

Product details

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

Dates and status

Registration Date: Nov 30, 2020
Expiry Date: Nov 30, 2025

About this record

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..

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