Taiwan FDA registration 38a35ebc764e688f3ba7b27a0a78f09a
"Edward" Finn-Fleck heparin-coated femoral arteriovenous catheter
TW: "愛德華"芬-弗列克肝素塗層股動靜脈導管
Taiwan·Risk Class 2·EDWARDS LIFESCIENCES LLC·Registered Nov 17, 2006 – Nov 17, 2016CancelledRegistration details
- Analysis ID
- 38a35ebc764e688f3ba7b27a0a78f09a
- Customs Code
- DHA00601743905
Company information
- Manufacturer
- EDWARDS LIFESCIENCES LLC
- Manufacturer Country
- United States
- Authorized Representative
- EDWARDS LIFESCIENCES (TAIWAN) CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.4210 Vascular catheters, cannulas and tubes for cardiopulmonary vascular bypassing
- Import Information
- import
Dates and status
- Registration Date
- Nov 17, 2006
- Expiry Date
- Nov 17, 2016
- Cancellation Date
- Apr 13, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Edward" Finn-Fleck heparin-coated femoral arteriovenous catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 38a35ebc764e688f3ba7b27a0a78f09a and manufactured by EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.
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