Taiwan FDA registration a0b9a2cb1f14ca89b774408e36a4910a
“Argon” Guidewire Introducer Needles
TW: “亞康恩”導引線導引針
Taiwan·Risk Class 2·MD·ARGON MEDICAL DEVICES INC.·Registered Feb 19, 2016 – Feb 19, 2026ExpiredRegistration details
- Analysis ID
- a0b9a2cb1f14ca89b774408e36a4910a
- License Form
- Ministry of Health Medical Device Import No. 028238
- Customs Code
- DHA05602823802
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)
- E1340 Catheter Guide
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 19, 2016
- Expiry Date
- Feb 19, 2026
About this record
Access comprehensive regulatory information for “Argon” Guidewire Introducer Needles in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a0b9a2cb1f14ca89b774408e36a4910a and manufactured by ARGON MEDICAL DEVICES INC.. The authorized representative in Taiwan is CHINA SPRING TRADING CO., LTD..
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