Taiwan FDA registration ebd3bdfaab2d7cacd7a5d92eeab8c915
“SIGKNOW” ECG Patch
TW: “準訊” 心電圖電極貼片
Taiwan·Risk Class 2·MD·SIGKNOW BIOMEDICAL CO., LTD.·Registered Jul 04, 2023 – Jul 04, 2028ActiveRegistration details
- Analysis ID
- ebd3bdfaab2d7cacd7a5d92eeab8c915
- License Form
- Ministry of Health Medical Device Manufacturing No. 007943
Company information
- Manufacturer
- SIGKNOW BIOMEDICAL CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SIGKNOW BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E2360 electrodes for ECG
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 04, 2023
- Expiry Date
- Jul 04, 2028
About this record
Access comprehensive regulatory information for “SIGKNOW” ECG Patch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ebd3bdfaab2d7cacd7a5d92eeab8c915 and manufactured by SIGKNOW BIOMEDICAL CO., LTD.. The authorized representative in Taiwan is SIGKNOW BIOMEDICAL 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