Taiwan FDA registration 7873d4307164a85909ed18f76fea7330
"Kaiden" Matilyn Benda coronary artery dilator stent system
TW: "凱登" 馬蒂琳奔達冠狀動脈擴張支架系統
Taiwan·GUIDANT IRELAND·Registered Oct 07, 2002 – Oct 07, 2007CancelledRegistration details
- Analysis ID
- 7873d4307164a85909ed18f76fea7330
- Customs Code
- DHA00601010608
Company information
- Manufacturer
- GUIDANT IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1310 經皮導管用血管擴張器
- Import Information
- import
Dates and status
- Registration Date
- Oct 07, 2002
- Expiry Date
- Oct 07, 2007
- Cancellation Date
- Nov 06, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kaiden" Matilyn Benda coronary artery dilator stent system in Taiwan's medical device market through Pure Global AI's free database. is registered under number 7873d4307164a85909ed18f76fea7330 and manufactured by GUIDANT IRELAND. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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