Taiwan FDA registration 9a2c7e7c558403208e31451e5a9eed47
"Medtronic" Aitan Stafi Lead
TW: “美敦力”艾坦史塔菲導線
Taiwan·Risk Class 2·MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA·Registered Jun 30, 2009 – Jun 30, 2019CancelledRegistration details
- Analysis ID
- 9a2c7e7c558403208e31451e5a9eed47
- Customs Code
- DHA00602002807
Company information
- Manufacturer
- MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA
- 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
- Import Information
- import
Dates and status
- Registration Date
- Jun 30, 2009
- Expiry Date
- Jun 30, 2019
- Cancellation Date
- Jun 16, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" Aitan Stafi Lead in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a2c7e7c558403208e31451e5a9eed47 and manufactured by MEDTRONIC PUERTO RICO OPERATIONS CO., VILLALBA. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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