Taiwan FDA registration 63c50fc218629630657b6801668d1e25
"Medtronic" aortic prosthetic vascular valve
TW: “美敦力”主動脈人工血管瓣膜
Taiwan·Risk Class 3·Medtronic Inc.·Registered Jun 26, 2012 – Jun 26, 2017CancelledRegistration details
- Analysis ID
- 63c50fc218629630657b6801668d1e25
- Customs Code
- DHA00602374001
Company information
- Manufacturer
- Medtronic Inc.
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.3925 Hypocardial membrane substitutions
- Import Information
- import
Dates and status
- Registration Date
- Jun 26, 2012
- Expiry Date
- Jun 26, 2017
- Cancellation Date
- Sep 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" aortic prosthetic vascular valve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 63c50fc218629630657b6801668d1e25 and manufactured by Medtronic Inc.. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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