Pure Global

“PROCEPT” AQUABEAM Robotic System - Taiwan Registration 4c427be234f55593ad787f4466e00985

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..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

Free Database
Powered by Pure Global AI
89,000+ Devices
4c427be234f55593ad787f4466e00985
Registration Details
Taiwan FDA Registration: 4c427be234f55593ad787f4466e00985
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“PROCEPT” AQUABEAM Robotic System
TW: “波塞頓”機械手臂水刀系統
Risk Class 2
MD

Registration Details

4c427be234f55593ad787f4466e00985

Ministry of Health Medical Device Import No. 035258

DHA05603525809

Company Information

United States

Product Details

This product is used to excision and remove prostate tissue to treat lower urinary tract symptoms caused by benign prostate hypertrophy.

H Gastroenterology and urology

H9999 Other

Imported from abroad

Dates and Status

May 03, 2022

May 03, 2027