Taiwan FDA registration aacb6739dd7febafedc2b8352768b1db
"Medtronic" cerebrospinal fluid ventricular reservoir
TW: "美敦力"腦脊髓液腦室儲液器
Registration details
- Analysis ID
- aacb6739dd7febafedc2b8352768b1db
- Customs Code
- DHA00601165507
Company information
- Manufacturer
- MEDTRONIC NEUROSURGERY
- Manufacturer Country
- United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.5550 Central nervous system fluid diverter and its components
- Import Information
- import
Dates and status
- Registration Date
- Aug 09, 2005
- Expiry Date
- Aug 09, 2015
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for "Medtronic" cerebrospinal fluid ventricular reservoir in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number aacb6739dd7febafedc2b8352768b1db and manufactured by MEDTRONIC NEUROSURGERY. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) 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