Taiwan FDA registration 77dda9965126e097909827f5fe3b27aa
"Medtronic" Indelon second generation laminated stent system
TW: “美敦力”茵德倫第二代覆膜支架系統
Taiwan·Risk Class 3·MEDTRONIC IRELAND·Registered Jun 19, 2013 – Jun 19, 2028ActiveRegistration details
- Analysis ID
- 77dda9965126e097909827f5fe3b27aa
- Customs Code
- DHA00602497800
Company information
- Manufacturer
- MEDTRONIC IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details Chinese change in the effectiveness of the approved copy of the imitation order: for details, as in the Chinese copy of the imitation order approved copy (the original copy of the imitation label approved copy on December 2, 104 was withdrawn and invalidated).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0006.
- Import Information
- Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.
Dates and status
- Registration Date
- Jun 19, 2013
- Expiry Date
- Jun 19, 2028
About this record
Access comprehensive regulatory information for "Medtronic" Indelon second generation laminated stent system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 77dda9965126e097909827f5fe3b27aa and manufactured by MEDTRONIC IRELAND. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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