Taiwan FDA registration dffa6796212972c1cdc356c14cb66e20
“Merit” HeRO Graft
TW: “美瑞特”英雄人工血管
Taiwan·Risk Class 2·MD·Merit Medical Systems, Inc.·Registered May 14, 2018 – May 14, 2028ActiveRegistration details
- Analysis ID
- dffa6796212972c1cdc356c14cb66e20
- License Form
- Ministry of Health Medical Device Import No. 030764
- Customs Code
- DHA05603076402
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)
- E3450 Vascular graft supplement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 14, 2018
- Expiry Date
- May 14, 2028
About this record
Access comprehensive regulatory information for “Merit” HeRO Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dffa6796212972c1cdc356c14cb66e20 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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