Taiwan FDA registration 312e817af74ea534b472ba600b6a959f
"Kaio" non-respiratory medical sprayer (unsterilized)
TW: "凱歐"非呼吸用醫藥噴霧器(未滅菌)
Taiwan·Risk Class 1·KOO MEDICAL·Registered Apr 12, 2013 – Apr 12, 2018CancelledRegistration details
- Analysis ID
- 312e817af74ea534b472ba600b6a959f
- Customs Code
- DHA04600187206
Company information
- Manufacturer
- KOO MEDICAL
- Manufacturer Country
- China
- Authorized Representative
- ASIACONNECT INTERNATIONAL COMPANY LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Non-respiratory Medical Aerosol Device (D.5640)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5640 非呼吸用醫藥噴霧器(atomizer)
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Apr 12, 2013
- Expiry Date
- Apr 12, 2018
- Cancellation Date
- Dec 20, 2019
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Kaio" non-respiratory medical sprayer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 312e817af74ea534b472ba600b6a959f and manufactured by KOO MEDICAL. The authorized representative in Taiwan is ASIACONNECT INTERNATIONAL COMPANY LTD..
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