Taiwan FDA registration 3f9924792744f3b533ea827bcbd0df35
"Abbot" Marklin coronary artery dilation catheter
TW: “亞培”馬克林冠狀動脈擴張導管
Taiwan·Risk Class 3·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Registered May 12, 2008 – May 12, 2013CancelledRegistration details
- Analysis ID
- 3f9924792744f3b533ea827bcbd0df35
- Customs Code
- DHA00601885409
Company information
- Manufacturer
- ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.)
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.0005.
- Import Information
- import
Dates and status
- Registration Date
- May 12, 2008
- Expiry Date
- May 12, 2013
- Cancellation Date
- Sep 26, 2016
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbot" Marklin coronary artery dilation catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 3f9924792744f3b533ea827bcbd0df35 and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is ABBOTT LABORATORIES SERVICES LLC TAIWAN BRANCH (U.S.A.).
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