Taiwan FDA registration 7857f62bf589fd826fe7acbe97f0fa68
"Meritt" laurel hydrophilic guide wire
TW: “美瑞特”桂冠親水性導引導線
Taiwan·Risk Class 2·MERIT MEDICAL IRELAND LIMITED·Registered Dec 29, 2011 – Dec 29, 2026ActiveRegistration details
- Analysis ID
- 7857f62bf589fd826fe7acbe97f0fa68
- Customs Code
- DHA00602318002
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 Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Dec 29, 2011
- Expiry Date
- Dec 29, 2026
About this record
Access comprehensive regulatory information for "Meritt" laurel 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 7857f62bf589fd826fe7acbe97f0fa68 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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