Taiwan FDA registration 251dcc88cc38ce8f96a8e3c61b98347c
"Cinda" blood collection needle (sterilization)
TW: "信達"採血針(滅菌)
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Oct 26, 2005 – Oct 26, 2010CancelledRegistration details
- Analysis ID
- 251dcc88cc38ce8f96a8e3c61b98347c
- Customs Code
- DHA04600001904
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- TYSON BIORESEARCH INC.
Product details
- Intended Use
- Minimally invasive skin tissue equipment for collection and examination.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Oct 26, 2005
- Expiry Date
- Oct 26, 2010
- Cancellation Date
- Jan 14, 2013
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Cinda" blood collection needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 251dcc88cc38ce8f96a8e3c61b98347c and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is TYSON BIORESEARCH INC..
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