Taiwan FDA registration 1ed20af71ea4e8721b96d8385a5f4b44
"Ekonti" Northby percutaneous cavity plasty balloon catheter
TW: “艾康蒂”諾斯比經皮穿腔成型術氣球導管
Taiwan·Risk Class 2·Acandis GmbH·Registered Jan 17, 2018 – Jan 17, 2028ActiveRegistration details
- Analysis ID
- 1ed20af71ea4e8721b96d8385a5f4b44
- Customs Code
- DHA05603070802
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
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1250 Percutaneous catheters
- Import Information
- import
Dates and status
- Registration Date
- Jan 17, 2018
- Expiry Date
- Jan 17, 2028
About this record
Access comprehensive regulatory information for "Ekonti" Northby percutaneous cavity plasty balloon catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ed20af71ea4e8721b96d8385a5f4b44 and manufactured by Acandis GmbH. The authorized representative in Taiwan is DR SHAO MD REGULATORY CONSULTANTS CO., LTD..
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