Taiwan FDA registration c3a7296b2dfc0189936b2298667a2d72
Kentelidov catheters
TW: 肯特利多芙導尿管
Taiwan·Risk Class 2·NELLCOR PURITAN BENNETT MEXICO S.A. DE C.V.·Registered Nov 08, 2005 – Nov 08, 2015CancelledRegistration details
- Analysis ID
- c3a7296b2dfc0189936b2298667a2d72
- Customs Code
- DHA00601294903
Company information
- Manufacturer
- NELLCOR PURITAN BENNETT MEXICO S.A. DE C.V.
- Manufacturer Country
- Mexico
- 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
- Import Information
- import
Dates and status
- Registration Date
- Nov 08, 2005
- Expiry Date
- Nov 08, 2015
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for Kentelidov catheters in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c3a7296b2dfc0189936b2298667a2d72 and manufactured by NELLCOR PURITAN BENNETT MEXICO S.A. DE C.V.. 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