Taiwan FDA registration dee69e28fd704344a1df0eef7b69a780
“Astek” Deluxe Double Interferential (IF) Current with Vacuum Therapy Apparatus
TW: “亞星”雙道式中頻向量\真空吸引機
Taiwan·Risk Class 2·MD·ASTEK TECHNOLOGY LTD.·Registered Jan 17, 2022 – Jan 17, 2027ActiveRegistration details
- Analysis ID
- dee69e28fd704344a1df0eef7b69a780
- License Form
- Ministry of Health Medical Device Manufacturing No. 007407
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ASTEK TECHNOLOGY LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O5850 powered muscle stimulator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jan 17, 2022
- Expiry Date
- Jan 17, 2027
About this record
Access comprehensive regulatory information for “Astek” Deluxe Double Interferential (IF) Current with Vacuum Therapy Apparatus in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dee69e28fd704344a1df0eef7b69a780 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