Taiwan FDA registration 60663ff73efb62bf8ab5b73d117f30b6
“Merit” SPLASHWire Hydrophilic Guide Wire
TW: “美瑞特” 史普勒斯親水性導引導線
Taiwan·Risk Class 2·MD·MERIT MEDICAL IRELAND LIMITED·Registered Apr 29, 2021 – Apr 29, 2026ExpiredRegistration details
- Analysis ID
- 60663ff73efb62bf8ab5b73d117f30b6
- License Form
- Ministry of Health Medical Device Import No. 034514
- Customs Code
- DHA05603451409
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
- Apr 29, 2021
- Expiry Date
- Apr 29, 2026
About this record
Access comprehensive regulatory information for “Merit” SPLASHWire Hydrophilic Guide Wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 60663ff73efb62bf8ab5b73d117f30b6 and manufactured by MERIT MEDICAL IRELAND LIMITED. 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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