Taiwan FDA registration 4c427be234f55593ad787f4466e00985
“PROCEPT” AQUABEAM Robotic System
TW: “波塞頓”機械手臂水刀系統
Taiwan·Risk Class 2·MD·Procept Biorobotics Corporation·Registered May 03, 2022 – May 03, 2027ActiveRegistration details
- Analysis ID
- 4c427be234f55593ad787f4466e00985
- License Form
- Ministry of Health Medical Device Import No. 035258
- Customs Code
- DHA05603525809
Company information
- Manufacturer
- Procept Biorobotics Corporation
- Manufacturer Country
- United States
- Authorized Representative
- DOUBLE-SUCCESS CO., LTD.
Product details
- Intended Use
- This product is used to excision and remove prostate tissue to treat lower urinary tract symptoms caused by benign prostate hypertrophy.
- Product Type (Level 1)
- H Gastroenterology and urology
- Product Type (Level 2)
- H9999 Other
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 03, 2022
- Expiry Date
- May 03, 2027
About this record
Access comprehensive regulatory information for “PROCEPT” AQUABEAM Robotic System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4c427be234f55593ad787f4466e00985 and manufactured by Procept Biorobotics Corporation. The authorized representative in Taiwan is DOUBLE-SUCCESS CO., LTD..
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