Taiwan FDA registration f82cc5250a2077a004be4fdfe97ebec8
"Kentley" Kuloti catheter
TW: “肯特利”庫洛帝導尿管
Taiwan·Risk Class 2·KENDALL- GAMMATRON CO., LTD.·Registered May 22, 2007 – May 22, 2012CancelledRegistration details
- Analysis ID
- f82cc5250a2077a004be4fdfe97ebec8
- Customs Code
- DHA00601809201
Company information
- Manufacturer
- KENDALL- GAMMATRON CO., LTD.
- Manufacturer Country
- Thailand
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H.5130 泌尿導管及其附件
- Import Information
- import
Dates and status
- Registration Date
- May 22, 2007
- Expiry Date
- May 22, 2012
- Cancellation Date
- Jul 25, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentley" Kuloti catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f82cc5250a2077a004be4fdfe97ebec8 and manufactured by KENDALL- GAMMATRON CO., LTD.. The authorized representative in Taiwan is Taiwan Covidien Corporation 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