Taiwan FDA registration 78d511faffa6cf5573f93ea3e5aa5b36
"Daylight" muscle stimulator
TW: "日光" 肌肉刺激器
Taiwan·Risk Class 2·ASTEK TECHNOLOGY LTD.·Registered Apr 18, 2022 – Apr 18, 2027ActiveRegistration details
- Analysis ID
- 78d511faffa6cf5573f93ea3e5aa5b36
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- YUAN-FOUNTAIN ENTERPRISE CO., 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)
- O.5850 5850.
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Apr 18, 2022
- Expiry Date
- Apr 18, 2027
About this record
Access comprehensive regulatory information for "Daylight" muscle stimulator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78d511faffa6cf5573f93ea3e5aa5b36 and manufactured by ASTEK TECHNOLOGY LTD.. The authorized representative in Taiwan is YUAN-FOUNTAIN ENTERPRISE 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