Taiwan FDA registration af5208d514b8d44381d67bd35f929a68
"Gaydon" Ezik-style carbon dioxide fog blower
TW: "蓋登" 艾齊克式二氧化碳吹霧器
Taiwan·Risk Class 1·GUIDANT CORPORATION CARDIAC SURGERY·Registered Jul 21, 2005 – Jul 21, 2010CancelledRegistration details
- Analysis ID
- af5208d514b8d44381d67bd35f929a68
- Customs Code
- DHA04400024905
Company information
- Manufacturer
- GUIDANT CORPORATION CARDIAC SURGERY
- Manufacturer Country
- United States
- Authorized Representative
- RAYING TECHNOLOGY COMPANY
Product details
- Intended Use
- It is used in coronary artery anastomosis surgery to remove blood from the anastomosis to increase the visibility of the surgical field.
- Product Type (Level 1)
- J General hospital and personal use equipment
- Import Information
- import
Dates and status
- Registration Date
- Jul 21, 2005
- Expiry Date
- Jul 21, 2010
- Cancellation Date
- Nov 16, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Gaydon" Ezik-style carbon dioxide fog blower in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af5208d514b8d44381d67bd35f929a68 and manufactured by GUIDANT CORPORATION CARDIAC SURGERY. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.
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