Taiwan FDA registration f35c01afbfcf2f503b97264f89b39f30
"Jiaxin" sputum extraction machine
TW: “佳新”抽痰機
Taiwan·Risk Class 2·JIA XIN MEDICAL & REHAB CO., LTD.·Registered Oct 12, 2007 – Oct 12, 2012CancelledRegistration details
- Analysis ID
- f35c01afbfcf2f503b97264f89b39f30
- Customs Code
- DHY00500228100
Company information
- Manufacturer
- JIA XIN MEDICAL & REHAB CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JIA XIN MEDICAL & REHAB CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.4780 動力式抽吸幫浦
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 12, 2007
- Expiry Date
- Oct 12, 2012
- Cancellation Date
- Nov 20, 2012
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Jiaxin" sputum extraction machine in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f35c01afbfcf2f503b97264f89b39f30 and manufactured by JIA XIN MEDICAL & REHAB CO., LTD.. The authorized representative in Taiwan is JIA XIN MEDICAL & REHAB CO., LTD..
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