Taiwan FDA registration a1b40ba9bcb2c491d06a23d88f499671
"Atrium" Andamax artificial blood vessels
TW: "心房" 安達麥克斯人工血管
Registration details
- Analysis ID
- a1b40ba9bcb2c491d06a23d88f499671
- Customs Code
- DHA00600980001
Company information
- Manufacturer
- ATRIUM MEDICAL CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Huangfa Co., Ltd
Product details
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Jan 09, 2002
- Expiry Date
- Jan 09, 2012
- Cancellation Date
- May 05, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Atrium" Andamax artificial blood vessels in Taiwan's medical device market through Pure Global AI's free database. is registered under number a1b40ba9bcb2c491d06a23d88f499671 and manufactured by ATRIUM MEDICAL CORPORATION. The authorized representative in Taiwan is Huangfa Co., Ltd.
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