Taiwan FDA registration 27738eb3e0020da731c63980594fb4d9
"Tripheus" aortic punch
TW: "特立菲斯"主動脈打孔器
Taiwan·Risk Class 1·TELEFLEX MEDICAL·Registered Nov 03, 2005 – Nov 03, 2010CancelledRegistration details
- Analysis ID
- 27738eb3e0020da731c63980594fb4d9
- Customs Code
- DHA04400171309
Company information
- Manufacturer
- TELEFLEX MEDICAL
- Manufacturer Country
- United States
- Authorized Representative
- HSIN TUNG MEDICAL CO., LTD.
Product details
- Intended Use
- Cardiovascular surgery instruments are surgical instruments with special functions for cardiovascular surgery.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4500 心臟血管外科器械
- Import Information
- import
Dates and status
- Registration Date
- Nov 03, 2005
- Expiry Date
- Nov 03, 2010
- Cancellation Date
- Dec 13, 2010
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Tripheus" aortic punch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 27738eb3e0020da731c63980594fb4d9 and manufactured by TELEFLEX MEDICAL. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..
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