Taiwan FDA registration a7afbda50bd8b51f7d030944f2e2cdc9
“Medtronic” Mosaic Bioprosthesis
TW: “美敦力”莫克生物性瓣膜
Taiwan·Risk Class 3·MD·MEDTRONIC HEART VALVES DIVISION·Registered Jun 22, 2016 – Jun 22, 2026ExpiredRegistration details
- Analysis ID
- a7afbda50bd8b51f7d030944f2e2cdc9
- License Form
- Ministry of Health Medical Device Import No. 028395
- Customs Code
- DHA05602839502
Company information
- Manufacturer
- MEDTRONIC HEART VALVES DIVISION
- 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 devices
- Product Type (Level 2)
- E3925 Heart valve replacement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 22, 2016
- Expiry Date
- Jun 22, 2026
About this record
Access comprehensive regulatory information for “Medtronic” Mosaic Bioprosthesis in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number a7afbda50bd8b51f7d030944f2e2cdc9 and manufactured by MEDTRONIC HEART VALVES DIVISION. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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