Taiwan FDA registration 37ab0c56034bb15a2bdf1789fea1fec7
“Edwards” OptiSite Arterial Perfusion Cannula
TW: “愛德華”動脈灌注導管
Taiwan·Risk Class 2·MD·EDWARDS LIFESCIENCES LLC.·Registered Aug 15, 2013 – Aug 15, 2028ActiveRegistration details
- Analysis ID
- 37ab0c56034bb15a2bdf1789fea1fec7
- License Form
- Ministry of Health Medical Device Import No. 025230
- Customs Code
- DHA05602523007
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 devices
- Product Type (Level 2)
- E1300 catheter cannula
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 15, 2013
- Expiry Date
- Aug 15, 2028
About this record
Access comprehensive regulatory information for “Edwards” OptiSite Arterial Perfusion Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 37ab0c56034bb15a2bdf1789fea1fec7 and manufactured by EDWARDS LIFESCIENCES LLC.. The authorized representative in Taiwan is EDWARDS LIFESCIENCES (TAIWAN) CORPORATION.
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