Taiwan FDA registration 4e1d635722cf14d97785dfe374d2a471
"Edward" femoral arterial/venous catheter group
TW: “愛德華”股動/靜脈導管組
Taiwan·Risk Class 2·EDWARDS LIFESCIENCES LLC.;; EDWARDS LIFESCIENCES LLC·Registered Apr 05, 2017 – Apr 05, 2027ActiveRegistration details
- Analysis ID
- 4e1d635722cf14d97785dfe374d2a471
- Customs Code
- DHA05602965201
Company information
- 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
- Input;; Contract manufacturing
Dates and status
- Registration Date
- Apr 05, 2017
- Expiry Date
- Apr 05, 2027
About this record
Access comprehensive regulatory information for "Edward" femoral arterial/venous catheter group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4e1d635722cf14d97785dfe374d2a471 and manufactured by EDWARDS LIFESCIENCES LLC.;; EDWARDS LIFESCIENCES LLC. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.
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