Taiwan FDA registration a4d5e829899af5d3abe3ccb427267a4c

"Ikeslan" locates the robot arm via a cranial magnetic stimulation coil

TW: “愛客思朗”經顱磁刺激線圈定位機器人手臂
Taiwan flagTaiwan·Risk Class 2·Axilum Robotics;; Weil Industries·Registered May 05, 2023 – May 05, 2028Active
Registration details
Analysis ID
a4d5e829899af5d3abe3ccb427267a4c
Customs Code
DHA05603649301
Company information
Manufacturer Country
France
Authorized Representative
TRUSHINE MEDICAL INSTRUMENT CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
K Neuroscience
Product Type (Level 2)
K.4560 Instruments for stereotaxic use of the nervous system; K.5805 Repetitive transcranial magnetic stimulation (rTMS) therapy system
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
May 05, 2023
Expiry Date
May 05, 2028
About this record

Access comprehensive regulatory information for "Ikeslan" locates the robot arm via a cranial magnetic stimulation coil in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a4d5e829899af5d3abe3ccb427267a4c and manufactured by Axilum Robotics;; Weil Industries. The authorized representative in Taiwan is TRUSHINE MEDICAL INSTRUMENT 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 DatabasePowered by Pure Global AI89,000+ Devices