Taiwan FDA registration 4a400514a4bb85144399ecb3985177c2
"Kentley" Madika intravenous cannula
TW: "肯特利"瑪迪卡靜脈內套管
Taiwan·TYCO HEALTHCARE (UK) MANUFACTURING LIMITED·Registered Feb 06, 2006 – Feb 06, 2011CancelledRegistration details
- Analysis ID
- 4a400514a4bb85144399ecb3985177c2
- Customs Code
- DHA00601393701
Company information
- Manufacturer
- TYCO HEALTHCARE (UK) MANUFACTURING LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Taiwan Tyco Pharmaceutical Co., Ltd
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5200 Endovascular catheters
- Import Information
- import
Dates and status
- Registration Date
- Feb 06, 2006
- Expiry Date
- Feb 06, 2011
- Cancellation Date
- Jan 18, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentley" Madika intravenous cannula in Taiwan's medical device market through Pure Global AI's free database. is registered under number 4a400514a4bb85144399ecb3985177c2 and manufactured by TYCO HEALTHCARE (UK) MANUFACTURING LIMITED. The authorized representative in Taiwan is Taiwan Tyco Pharmaceutical 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