Taiwan FDA registration 158ce4cbff47c0d27cf152b211b2ab85
“Argon” WORKER Guidewires
TW: “亞康恩”握科導引線
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES, INC.·Registered Dec 23, 2014 – Dec 23, 2024ExpiredRegistration details
- Analysis ID
- 158ce4cbff47c0d27cf152b211b2ab85
- License Form
- Ministry of Health Medical Device Import No. 026916
- Customs Code
- DHA05602691607
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 devices
- Product Type (Level 2)
- E1330 Catheter Lead
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 23, 2014
- Expiry Date
- Dec 23, 2024
About this record
Access comprehensive regulatory information for “Argon” WORKER Guidewires in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 158ce4cbff47c0d27cf152b211b2ab85 and manufactured by ARGON MEDICAL DEVICES, INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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