Taiwan FDA registration c586738196b56fe05ea96fc8a4f476c5
“geko” neuromuscular electrical stimulation device
TW: “格酷”神經肌肉電刺激裝置
Taiwan·Risk Class 2·MD·Firstkind Limited·Registered Jun 01, 2020 – Jun 01, 2025ExpiredRegistration details
- Analysis ID
- c586738196b56fe05ea96fc8a4f476c5
- License Form
- Ministry of Health Medical Device Import No. 033802
- Customs Code
- DHA05603380209
Company information
- Manufacturer
- Firstkind Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- REGISTAR CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 01, 2020
- Expiry Date
- Jun 01, 2025
About this record
Access comprehensive regulatory information for “geko” neuromuscular electrical stimulation device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c586738196b56fe05ea96fc8a4f476c5 and manufactured by Firstkind Limited. The authorized representative in Taiwan is REGISTAR CO., LTD..
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