Taiwan FDA registration ef9f855e5980e4cfd764b56dfa33a63f
“Argon” Cleaner Rotational Thrombectomy Device
TW: “雅客”血栓旋轉清除器
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Nov 03, 2017 – Nov 03, 2027ActiveRegistration details
- Analysis ID
- ef9f855e5980e4cfd764b56dfa33a63f
- License Form
- Ministry of Health Medical Device Import No. 030409
- Customs Code
- DHA05603040905
Company information
- Manufacturer
- ARGON MEDICAL DEVICES, INC.
- Manufacturer Country
- United States
- Authorized Representative
- JENS MEDICAL CONSULTING LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E5150 Thrombectomy catheter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 03, 2017
- Expiry Date
- Nov 03, 2027
About this record
Access comprehensive regulatory information for “Argon” Cleaner Rotational Thrombectomy Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ef9f855e5980e4cfd764b56dfa33a63f and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is JENS MEDICAL CONSULTING LTD..
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