Taiwan FDA registration 430b8b35675361647c0f3e442a071087
“Merit” SeaDragon Torque Device
TW: “美瑞特” 海龍控線器組
Taiwan·Risk Class 2·MD·Merit Medical Systems, Inc.·Registered Sep 16, 2013 – Sep 16, 2028ActiveRegistration details
- Analysis ID
- 430b8b35675361647c0f3e442a071087
- License Form
- Ministry of Health Medical Device Import No. 025242
- Customs Code
- DHA05602524201
Company information
- Manufacturer
- Merit Medical Systems, Inc.
- Manufacturer Country
- United States
- 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
- Sep 16, 2013
- Expiry Date
- Sep 16, 2028
About this record
Access comprehensive regulatory information for “Merit” SeaDragon Torque Device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 430b8b35675361647c0f3e442a071087 and manufactured by Merit Medical Systems, Inc.. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
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