Taiwan FDA registration ca2ae7a20470c6afa08cb4a93caf4d43

"Gibeo" electrotherapy instrument

TW: “吉貝歐”電療儀
Taiwan flagTaiwan·Risk Class 2·GBO MEDIZINTECHNIK AG.·Registered Feb 14, 2022 – Feb 14, 2027Active
Registration details
Analysis ID
ca2ae7a20470c6afa08cb4a93caf4d43
Customs Code
DHA05603530301
Company information
Manufacturer Country
Germany
Authorized Representative
DYNO-TEC TECHNOLOGY INC.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
K Neuroscience;;O Physical Medical Sciences
Product Type (Level 2)
K.5890 Transcutaneous electrical nerve stimulator for pain relief; O.5850 Powered Muscle Stimulator
Import Information
import
Dates and status
Registration Date
Feb 14, 2022
Expiry Date
Feb 14, 2027
Companies making similar products

Top companies providing products similar to ""Gibeo" electrotherapy instrument"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Gibeo" electrotherapy instrument in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca2ae7a20470c6afa08cb4a93caf4d43 and manufactured by GBO MEDIZINTECHNIK AG.. The authorized representative in Taiwan is DYNO-TEC TECHNOLOGY INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GBO MEDIZINTECHNIK AG., and 2 recent registrations in the same category. 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+ Devices1 Competitors2 Recent Registrations