Taiwan FDA registration 683f7a9f674db6ec09c474985296b641
"Ecanti" Credor Bracket
TW: “艾康蒂” 克蕾朵支架
Taiwan·Risk Class 3·Acandis GmbH·Registered Jul 30, 2019 – Jul 30, 2029ActiveRegistration details
- Analysis ID
- 683f7a9f674db6ec09c474985296b641
- Customs Code
- DHA05603161401
Company information
- Manufacturer
- Acandis GmbH
- Manufacturer Country
- Germany
- Authorized Representative
- DR SHAO MD REGULATORY CONSULTANTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order. Indication changes: Details as approved Chinese instructions (the labels, instructions or packaging originally approved on December 3, 110 will be recycled and scrapped).
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.0001 Cardiovascular stents
- Import Information
- Safety monitoring;; import
Dates and status
- Registration Date
- Jul 30, 2019
- Expiry Date
- Jul 30, 2029
About this record
Access comprehensive regulatory information for "Ecanti" Credor Bracket in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 683f7a9f674db6ec09c474985296b641 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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