Taiwan FDA registration b342b64b1c2f74adb8c119b8a506aba3
"Medtronic" Dipp reverse coronal sinus perfusion cannula
TW: "美敦力" 帝普逆向冠狀竇灌流套管
Taiwan·Risk Class 2·Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS·Registered Jul 29, 2002 – Jul 29, 2027ActiveRegistration details
- Analysis ID
- b342b64b1c2f74adb8c119b8a506aba3
- Customs Code
- DHA00601000400
Company information
- Manufacturer
- Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1300 Guide Tube Casing
- Import Information
- import
Dates and status
- Registration Date
- Jul 29, 2002
- Expiry Date
- Jul 29, 2027
About this record
Access comprehensive regulatory information for "Medtronic" Dipp reverse coronal sinus perfusion cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b342b64b1c2f74adb8c119b8a506aba3 and manufactured by Medtronic Inc.;; MEDTRONIC PERFUSION SYSTEMS. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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