Taiwan FDA registration 0a43391903eb9c14f644e525f666df7b
"Medtronic" Cape Summer Rectification Wire
TW: "美敦力" 開普夏整律導線
Taiwan·Risk Class 3·MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA·Registered Jul 16, 2002 – Jul 16, 2022CancelledRegistration details
- Analysis ID
- 0a43391903eb9c14f644e525f666df7b
- Customs Code
- DHA00600998701
Company information
- Manufacturer
- MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jul 16, 2002
- Expiry Date
- Jul 16, 2022
- Cancellation Date
- Mar 14, 2019
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Medtronic" Cape Summer Rectification Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 0a43391903eb9c14f644e525f666df7b and manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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