Taiwan FDA registration 0f71e44099f7fb611e4eb70fa9e71abb
"Maya 2nd generation" physiological parameter box
TW: “馬雅2代”生理參數匣道器
Taiwan·Risk Class 2·WISTRON CORPORATION·Registered Sep 19, 2017 – Sep 19, 2027ActiveRegistration details
- Analysis ID
- 0f71e44099f7fb611e4eb70fa9e71abb
Company information
- Manufacturer
- WISTRON CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MAYAMINER COMPANY LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2910 無線電波式生理信號傳輸接收器
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Sep 19, 2017
- Expiry Date
- Sep 19, 2027
About this record
Access comprehensive regulatory information for "Maya 2nd generation" physiological parameter box in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0f71e44099f7fb611e4eb70fa9e71abb and manufactured by WISTRON CORPORATION. The authorized representative in Taiwan is MAYAMINER COMPANY 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