Taiwan FDA registration 2f0ef50f3cdd76d91c8a7f569b47dbf1
“Merit” InQwire AMPLATZ Guide Wires
TW: “美瑞特”安普拉斯導引導線
Taiwan·Risk Class 2·MD·MERIT MEDICAL IRELAND LIMITED·Registered Mar 13, 2020 – Mar 13, 2025ExpiredRegistration details
- Analysis ID
- 2f0ef50f3cdd76d91c8a7f569b47dbf1
- License Form
- Ministry of Health Medical Device Import No. 033317
- Customs Code
- DHA05603331702
Company information
- Manufacturer
- MERIT MEDICAL IRELAND LIMITED
- Manufacturer Country
- Ireland
- Authorized Representative
- Merit Medical Asia Company Limited Taiwan Branch (Hong Kong)
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
- Mar 13, 2020
- Expiry Date
- Mar 13, 2025
About this record
Access comprehensive regulatory information for “Merit” InQwire AMPLATZ Guide Wires in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f0ef50f3cdd76d91c8a7f569b47dbf1 and manufactured by MERIT MEDICAL IRELAND LIMITED. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).
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