Taiwan FDA registration 211fb0242f6708aa04013e3c8dadfc17
"Astek" Limb Protector (Non-Sterile)
TW: "亞星" 肢體護具 (未滅菌)
Taiwan·Risk Class 1·MD·ASTEK TECHNOLOGY LTD.·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- 211fb0242f6708aa04013e3c8dadfc17
- License Form
- Ministry of Health Medical Device Manufacturing Registration No. 005770
Company information
- Manufacturer
- ASTEK TECHNOLOGY LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ASTEK TECHNOLOGY LTD.
Product details
- Intended Use
- Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- o Equipment for physical medicine
- Product Type (Level 2)
- O3475 Body Equipment
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for "Astek" Limb Protector (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 211fb0242f6708aa04013e3c8dadfc17 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