Taiwan FDA registration 7213c53cdcd7d4cd67f5dd7b8f25ae2e
"Caudis" Parmas biliary stent
TW: “考迪斯”帕瑪士膽道支架
Registration details
- Analysis ID
- 7213c53cdcd7d4cd67f5dd7b8f25ae2e
- Customs Code
- DHA00602275904
Company information
- Manufacturer
- CORDIS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5010 膽管用導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- Aug 24, 2011
- Expiry Date
- Aug 24, 2026
About this record
Access comprehensive regulatory information for "Caudis" Parmas biliary stent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7213c53cdcd7d4cd67f5dd7b8f25ae2e and manufactured by CORDIS CORPORATION. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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