Taiwan FDA registration 72723aed191cd1ec8dc612854a31ad56
“MESI” mTABLET ECG diagnostic system
TW: 〝梅西〞心電圖機
Taiwan·Risk Class 2·MD·MESI, development of medical devices, LTD.·Registered May 31, 2022 – May 31, 2027ActiveRegistration details
- Analysis ID
- 72723aed191cd1ec8dc612854a31ad56
- License Form
- Ministry of Health Medical Device Import No. 035444
- Customs Code
- DHA05603544406
Company information
- Manufacturer
- MESI, development of medical devices, LTD.
- Manufacturer Country
- Slovenia
- Authorized Representative
- PINYORK INSTRUMENTS 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)
- E2340 ECG Scanner
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 31, 2022
- Expiry Date
- May 31, 2027
About this record
Access comprehensive regulatory information for “MESI” mTABLET ECG diagnostic system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72723aed191cd1ec8dc612854a31ad56 and manufactured by MESI, development of medical devices, LTD.. The authorized representative in Taiwan is PINYORK INSTRUMENTS CO., LTD..
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