Taiwan FDA registration 4f8af7a5a0bf48ca4874b147d81dd797
Lung mesh (biovascular)
TW: 肺補片（生物血管）
Taiwan·BIO-VASCULAR, INC.·Registered Dec 13, 1997 – Dec 13, 2002CancelledRegistration details
- Analysis ID
- 4f8af7a5a0bf48ca4874b147d81dd797
- Customs Code
- DHA00600816608
Company information
- Manufacturer
- BIO-VASCULAR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- Swiss company Keith & Co., Ltd. Taipei Branch
Product details
- Intended Use
- Vacuum.
- Product Type (Level 1)
- 0300 Prosthetic function substitute
- Import Information
- import
Dates and status
- Registration Date
- Dec 13, 1997
- Expiry Date
- Dec 13, 2002
- Cancellation Date
- Aug 30, 2007
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Lung mesh (biovascular) in Taiwan's medical device market through Pure Global AI's free database. is registered under number 4f8af7a5a0bf48ca4874b147d81dd797 and manufactured by BIO-VASCULAR, INC.. The authorized representative in Taiwan is Swiss company Keith & Co., Ltd. Taipei 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