Taiwan FDA registration 9fefe44454965fff16bb383d2f53edba
"Yakan" Ekun Ekoff's intravascular retrieval kit
TW: “亞康恩”埃璀夫血管內取物器套件
Taiwan·Risk Class 2·ARGON MEDICAL DEVICES INC.·Registered Sep 19, 2011 – Sep 19, 2026ActiveRegistration details
- Analysis ID
- 9fefe44454965fff16bb383d2f53edba
- Customs Code
- DHA00602281208
Company information
- Manufacturer
- ARGON MEDICAL DEVICES INC.
- Manufacturer Country
- United States
- Authorized Representative
- CHINA SPRING TRADING 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.5150 血栓切除術導管
- Import Information
- import
Dates and status
- Registration Date
- Sep 19, 2011
- Expiry Date
- Sep 19, 2026
About this record
Access comprehensive regulatory information for "Yakan" Ekun Ekoff's intravascular retrieval kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fefe44454965fff16bb383d2f53edba and manufactured by ARGON MEDICAL DEVICES INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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