Taiwan FDA registration fdc3ccc5544fcc90fc81cc89b8fd889b
"Bebi" focuses on the ultrasound system
TW: “蓓比”聚焦超音波系統
Taiwan·Risk Class 2·BE&BI Tech Co.·Registered Nov 19, 2024 – Nov 19, 2029ActiveRegistration details
- Analysis ID
- fdc3ccc5544fcc90fc81cc89b8fd889b
- Customs Code
- DHA05603765605
Company information
- Manufacturer
- BE&BI Tech Co.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PRIMESTAR MEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- I General, Plastic Surgery and Dermatology
- Product Type (Level 2)
- I.0008 Percutaneous skin stimulator
- Import Information
- import
Dates and status
- Registration Date
- Nov 19, 2024
- Expiry Date
- Nov 19, 2029
About this record
Access comprehensive regulatory information for "Bebi" focuses on the ultrasound system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fdc3ccc5544fcc90fc81cc89b8fd889b and manufactured by BE&BI Tech Co.. The authorized representative in Taiwan is PRIMESTAR MEDICAL CO., LTD..
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