Taiwan FDA registration 2f1fcfab1c5969e8f60fef8927463bda
“ASTEK” ELECTROCONDUCTIVE PAD
TW: “亞星”電極貼片
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Apr 04, 2019 – Apr 04, 2024ExpiredRegistration details
- Analysis ID
- 2f1fcfab1c5969e8f60fef8927463bda
- License Form
- Ministry of Health Medical Device Manufacturing No. 006332
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ASTEK TECHNOLOGY 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)
- K1320 skin electrode
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 04, 2019
- Expiry Date
- Apr 04, 2024
About this record
Access comprehensive regulatory information for “ASTEK” ELECTROCONDUCTIVE PAD in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2f1fcfab1c5969e8f60fef8927463bda and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is ASTEK TECHNOLOGY 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