Taiwan FDA registration c899ae43104b669027ddb5503a8ffa66
H2 Plus Wearable ECG Recorder
TW: 麗臺穿戴心電圖記錄器
Registration details
- Analysis ID
- c899ae43104b669027ddb5503a8ffa66
- License Form
- Ministry of Health Medical Device Manufacturing No. 006790
Company information
- Manufacturer
- LEADTEK RESEARCH, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- LEADTEK RESEARCH, INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2340 ECG Scanner
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 13, 2020
- Expiry Date
- May 13, 2025
About this record
Access comprehensive regulatory information for H2 Plus Wearable ECG Recorder in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c899ae43104b669027ddb5503a8ffa66 and manufactured by LEADTEK RESEARCH, INC.. The authorized representative in Taiwan is LEADTEK RESEARCH, INC..
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