Taiwan FDA registration 79fb7b2af04f75667f5bc77070406b1d
“KAIXIN” Bladder Scanner
TW: “凱信”膀胱掃描儀
Taiwan·Risk Class 2·MD·Xuzhou Kaixin Electronic Instrument Co., Ltd.·Registered Aug 02, 2019 – Aug 02, 2024ExpiredRegistration details
- Analysis ID
- 79fb7b2af04f75667f5bc77070406b1d
- License Form
- Ministry of Health Medical Device Land Transport No. 001056
- Customs Code
- DHA09200105602
Company information
- Manufacturer
- Xuzhou Kaixin Electronic Instrument Co., Ltd.
- Manufacturer Country
- China
- Authorized Representative
- INNOFUTURE INTERNATIONAL INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P1560 ultrasonic echo imaging system
- Import Information
- Imported from abroad; Made in China
Dates and status
- Registration Date
- Aug 02, 2019
- Expiry Date
- Aug 02, 2024
About this record
Access comprehensive regulatory information for “KAIXIN” Bladder Scanner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79fb7b2af04f75667f5bc77070406b1d and manufactured by Xuzhou Kaixin Electronic Instrument Co., Ltd.. The authorized representative in Taiwan is INNOFUTURE INTERNATIONAL INC..
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