Taiwan FDA registration c0c6d555b627f4699288267d426bf166
“Geltek-Medica” Unipaste conductive adhesive electrode paste
TW: “膠護美”優力配導電膠
Taiwan·Risk Class 2·MD·Geltek-Medica Ltd.·Registered Jul 24, 2020 – Jul 24, 2025ExpiredRegistration details
- Analysis ID
- c0c6d555b627f4699288267d426bf166
- License Form
- Ministry of Health Medical Device Import No. 033812
- Customs Code
- DHA05603381202
Company information
- Manufacturer
- Geltek-Medica Ltd.
- Manufacturer Country
- Russian Federation
- Authorized Representative
- AMY GRANT LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K1275 conductive medium
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 24, 2020
- Expiry Date
- Jul 24, 2025
About this record
Access comprehensive regulatory information for “Geltek-Medica” Unipaste conductive adhesive electrode paste in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c0c6d555b627f4699288267d426bf166 and manufactured by Geltek-Medica Ltd.. The authorized representative in Taiwan is AMY GRANT LTD..
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