Taiwan FDA registration eb25bd34c25a7cf828324427e63b5ab6
"Keithley" Ender Lilly implanted with fibrillation wires
TW: "吉時利" 恩德禮來內植除顫導線
Taiwan·GUIDANT IRELAND·Registered Sep 12, 2002 – Apr 21, 2010CancelledRegistration details
- Analysis ID
- eb25bd34c25a7cf828324427e63b5ab6
- Customs Code
- DHA00601007602
Company information
- Manufacturer
- GUIDANT IRELAND
- Manufacturer Country
- Ireland
- Authorized Representative
- Xiongqun Enterprise Limited
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.1330 Catheter Guide Wires
- Import Information
- import
Dates and status
- Registration Date
- Sep 12, 2002
- Expiry Date
- Apr 21, 2010
- Cancellation Date
- Oct 26, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Keithley" Ender Lilly implanted with fibrillation wires in Taiwan's medical device market through Pure Global AI's free database. is registered under number eb25bd34c25a7cf828324427e63b5ab6 and manufactured by GUIDANT IRELAND. The authorized representative in Taiwan is Xiongqun Enterprise Limited.
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