Taiwan FDA registration 227396664c4b06ff9482e798f5340f05
Funai conductive gel patch
TW: 船井傳導凝膠貼片
Taiwan·Risk Class 2·EVERYWAY MEDICAL INSTRUMENTS CO., LTD.·Registered Apr 27, 2020 – Apr 27, 2025ExpiredRegistration details
- Analysis ID
- 227396664c4b06ff9482e798f5340f05
Company information
- Manufacturer
- EVERYWAY MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- FUNCARE OF TAIWAN CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Neuroscience
- Product Type (Level 2)
- K.1320 Skin electrode
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 27, 2020
- Expiry Date
- Apr 27, 2025
About this record
Access comprehensive regulatory information for Funai conductive gel patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 227396664c4b06ff9482e798f5340f05 and manufactured by EVERYWAY MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is FUNCARE OF TAIWAN 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