Taiwan FDA registration 89a6479492c056264e3b06d893c7f593
"Kentley" Dove Sheevy catheter
TW: “肯特利”多芙席維導尿管
Taiwan·Risk Class 2·NELLCOR PURITAN BENNETT MEXICO S.A. DE C.V.·Registered Sep 05, 2008 – Sep 05, 2013CancelledRegistration details
- Analysis ID
- 89a6479492c056264e3b06d893c7f593
- Customs Code
- DHA00601920200
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
- Sep 05, 2008
- Expiry Date
- Sep 05, 2013
- Cancellation Date
- Apr 23, 2015
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Kentley" Dove Sheevy catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 89a6479492c056264e3b06d893c7f593 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