Taiwan FDA registration b568b9e8d58713a04088dd47375749b3
“Thoratec” CentriMag Cannula Kits
TW: “索羅格”善翠美血液套管組
Taiwan·Risk Class 2·MD·Thoratec Switzerland GmbH·Registered Jan 24, 2018 – Jan 24, 2028ActiveRegistration details
- Analysis ID
- b568b9e8d58713a04088dd47375749b3
- License Form
- Ministry of Health Medical Device Import No. 030714
- Customs Code
- DHA05603071400
Company information
- Manufacturer
- Thoratec Switzerland GmbH
- Manufacturer Country
- Switzerland
- Authorized Representative
- Abbott Medical Taiwan Co.
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)
- E4210 Vascular catheters, cannula and tubes for cardiopulmonary vascular bypass
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 24, 2018
- Expiry Date
- Jan 24, 2028
About this record
Access comprehensive regulatory information for “Thoratec” CentriMag Cannula Kits in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b568b9e8d58713a04088dd47375749b3 and manufactured by Thoratec Switzerland GmbH. The authorized representative in Taiwan is Abbott Medical Taiwan Co..
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