Taiwan FDA registration e60fd0e1a4773d48be5aa82b878f94df
Hinda blood collection pen and blood lancet needle
TW: 欣達採血筆及採血針
Taiwan·Risk Class 1·WUXI XINDA MEDICAL DEVICE CO., LTD·Registered Aug 06, 2007 – Aug 06, 2012CancelledRegistration details
- Analysis ID
- e60fd0e1a4773d48be5aa82b878f94df
- Customs Code
- DHA04600041308
Company information
- Manufacturer
- WUXI XINDA MEDICAL DEVICE CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- HMD BIOMEDICAL INC.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4800 Hand Instruments for General Surgery
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Aug 06, 2007
- Expiry Date
- Aug 06, 2012
- Cancellation Date
- Apr 30, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Hinda blood collection pen and blood lancet needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e60fd0e1a4773d48be5aa82b878f94df and manufactured by WUXI XINDA MEDICAL DEVICE CO., LTD. The authorized representative in Taiwan is HMD BIOMEDICAL INC..
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