Taiwan FDA registration d8a81002c7112d65142a061c57a3df51
"Abbott" Josden peripheral vascular enveloped stents
TW: 〝亞培〞喬斯登週邊血管包覆支架
Taiwan·Risk Class 2·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Registered Sep 30, 2000 – Sep 30, 2015CancelledRegistration details
- Analysis ID
- d8a81002c7112d65142a061c57a3df51
- Customs Code
- DHA00600951502
Company information
- Manufacturer
- ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Sep 30, 2000
- Expiry Date
- Sep 30, 2015
- Cancellation Date
- Jun 26, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbott" Josden peripheral vascular enveloped stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d8a81002c7112d65142a061c57a3df51 and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS CO., LTD..
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