Taiwan FDA registration 51a760f7af73ff82f3c66ca6eb6139b6
"Intergrama" Novi standard and pediatric shunt catheters
TW: "英特葛拉" 諾維氏標準及小兒分流導管
Registration details
- Analysis ID
- 51a760f7af73ff82f3c66ca6eb6139b6
- Customs Code
- DHA00601361607
Company information
- Manufacturer
- INTEGRA NEURO SCIENCES PR, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WONDERFUL INSTRUMENTS COMPANY, 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
- Nov 21, 2005
- Expiry Date
- Nov 21, 2010
- 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 "Intergrama" Novi standard and pediatric shunt catheters in Taiwan's medical device market through Pure Global AI's free database. is registered under number 51a760f7af73ff82f3c66ca6eb6139b6 and manufactured by INTEGRA NEURO SCIENCES PR, INC.. The authorized representative in Taiwan is WONDERFUL INSTRUMENTS COMPANY, 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