Taiwan FDA registration 4638688afb22917c56bc934ad99ad66c
“Mortara” Resting Electrocardiograph
TW: “摩托拉”心電圖機
Taiwan·Risk Class 2·MD·MORTARA INSTRUMENT, INC.·Registered Apr 19, 2019 – Apr 19, 2024ExpiredRegistration details
- Analysis ID
- 4638688afb22917c56bc934ad99ad66c
- License Form
- Ministry of Health Medical Device Import No. 032576
- Customs Code
- DHA05603257608
Company information
- Manufacturer
- MORTARA INSTRUMENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WISDOM UNION ENTERPRISE CO., LTD.
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
- Imported from abroad
Dates and status
- Registration Date
- Apr 19, 2019
- Expiry Date
- Apr 19, 2024
About this record
Access comprehensive regulatory information for “Mortara” Resting Electrocardiograph in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4638688afb22917c56bc934ad99ad66c and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
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