Taiwan FDA registration ebac3c51e12b854337577c461393e1a4
"Abbott" angiogram catheter
TW: "亞培" 血管攝影導管
Taiwan·ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH·Registered Dec 08, 2005 – Dec 08, 2010CancelledRegistration details
- Analysis ID
- ebac3c51e12b854337577c461393e1a4
- Customs Code
- DHA00601377402
Company information
- Manufacturer
- ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- WATTCAN INSTRUMENTS CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Import Information
- import
Dates and status
- Registration Date
- Dec 08, 2005
- Expiry Date
- Dec 08, 2010
- Cancellation Date
- Oct 25, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Abbott" angiogram catheter in Taiwan's medical device market through Pure Global AI's free database. is registered under number ebac3c51e12b854337577c461393e1a4 and manufactured by ABBOTT VASCULAR INSTRUMENTS DEUTSCHLAND GMBH. The authorized representative in Taiwan is WATTCAN INSTRUMENTS 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