Taiwan FDA registration 1f8bf4cffe4ca2dabd21d44a0beb2f0a
"Abbott" Josden coronary artery enveloped stents
TW: “亞培”喬斯登冠狀動脈包覆支架
Taiwan·Risk Class 3·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Registered Nov 23, 2011 – Nov 23, 2016CancelledRegistration details
- Analysis ID
- 1f8bf4cffe4ca2dabd21d44a0beb2f0a
- Customs Code
- DHA00602293307
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.0001 Cardiovascular stents
- Import Information
- import
Dates and status
- Registration Date
- Nov 23, 2011
- Expiry Date
- Nov 23, 2016
- Cancellation Date
- Aug 09, 2018
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Abbott" Josden coronary artery enveloped stents in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1f8bf4cffe4ca2dabd21d44a0beb2f0a 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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