Taiwan FDA registration b3dd565d3d20fbdc21b3fcb16b078765
"McVier" platinum double velvet artificial blood vessels
TW: "邁柯唯" 白金雙重絲絨人工血管
Taiwan·MAQUET CARDIOVASCULAR LLC·Registered Dec 27, 2002 – Dec 27, 2012CancelledRegistration details
- Analysis ID
- b3dd565d3d20fbdc21b3fcb16b078765
- Customs Code
- DHA00601016001
Company information
- Manufacturer
- MAQUET CARDIOVASCULAR LLC
- Manufacturer Country
- United States
- Authorized Representative
- Hong Kong Synmei Co., Ltd. Taiwan Branch
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Dec 27, 2002
- Expiry Date
- Dec 27, 2012
- Cancellation Date
- Mar 20, 2013
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "McVier" platinum double velvet artificial blood vessels in Taiwan's medical device market through Pure Global AI's free database. is registered under number b3dd565d3d20fbdc21b3fcb16b078765 and manufactured by MAQUET CARDIOVASCULAR LLC. The authorized representative in Taiwan is Hong Kong Synmei Co., Ltd. Taiwan Branch.
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