Taiwan FDA registration db1c9de46673cae59124b54992f3b539
Azik's vacuum suction type 2nd generation stabilizer series
TW: 艾齊克氏真空吸引式第二代穩定器系列
Taiwan·Risk Class 1·GUIDANT CORPORATION CARDIAC SURGERY·Registered Oct 03, 2005 – Oct 03, 2010CancelledRegistration details
- Analysis ID
- db1c9de46673cae59124b54992f3b539
- Customs Code
- DHA04400071406
Company information
- Manufacturer
- GUIDANT CORPORATION CARDIAC SURGERY
- Manufacturer Country
- United States
- Authorized Representative
- RAYING TECHNOLOGY COMPANY
Product details
- Intended Use
- A surgical instrument with a special function for cardiovascular surgery.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
Dates and status
- Registration Date
- Oct 03, 2005
- Expiry Date
- Oct 03, 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 Azik's vacuum suction type 2nd generation stabilizer series in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number db1c9de46673cae59124b54992f3b539 and manufactured by GUIDANT CORPORATION CARDIAC SURGERY. The authorized representative in Taiwan is RAYING TECHNOLOGY COMPANY.
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