Taiwan FDA registration dd17cf289a356471c206a9ec846e7ec3
"Medtronic" tourniquet set (sterilized)
TW: "美敦力" 止血帶組 (滅菌)
Taiwan·Risk Class 1·Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS·Registered Sep 14, 2005 – Sep 14, 2025ExpiredRegistration details
- Analysis ID
- dd17cf289a356471c206a9ec846e7ec3
- Customs Code
- DHA04400043900
Company information
- Manufacturer
- Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- During cardiopulmonary bypass surgery, a cardiopulmonary bypass cannula is immobilized.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4200 心肺血管繞道術輔助設備
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 2005
- Expiry Date
- Sep 14, 2025
About this record
Access comprehensive regulatory information for "Medtronic" tourniquet set (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dd17cf289a356471c206a9ec846e7ec3 and manufactured by Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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