Taiwan FDA registration 81ff3c42107d4ab198eb7cd0a66cf61d
"Merit" Flow can develop a guide sheath
TW: “美瑞特”福祿可顯影導引鞘
Registration details
- Analysis ID
- 81ff3c42107d4ab198eb7cd0a66cf61d
- Customs Code
- DHA00602231201
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 Medicine Science
- Product Type (Level 2)
- E.1340 Catheter Introducers
- Import Information
- import
Dates and status
- Registration Date
- May 16, 2011
- Expiry Date
- May 16, 2026
About this record
Access comprehensive regulatory information for "Merit" Flow can develop a guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81ff3c42107d4ab198eb7cd0a66cf61d 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.
Free DatabasePowered by Pure Global AI89,000+ Devices