Taiwan FDA registration 5300a76d20e95eca11949347da4ecf47
Siliceous obstruction spherical duct
TW: 矽質阻塞球形導管
Taiwan·AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION·Registered Apr 18, 1994 – Apr 18, 1999CancelledRegistration details
- Analysis ID
- 5300a76d20e95eca11949347da4ecf47
- Customs Code
- DHA00600717402
Company information
- Manufacturer
- AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- Swiss company Keith & Co., Ltd. Taipei Branch
Product details
- Product Type (Level 1)
- 0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment
Dates and status
- Registration Date
- Apr 18, 1994
- Expiry Date
- Apr 18, 1999
- 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 Siliceous obstruction spherical duct in Taiwan's medical device market through Pure Global AI's free database. is registered under number 5300a76d20e95eca11949347da4ecf47 and manufactured by AMERICAN BIOMED, INCORPORATED-CATHLAB DIVISION. 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