Taiwan FDA registration 1a9afaa3d4822ff39dcb49a3daf0eabc
"Motorola" telemetry monitoring center software
TW: “摩托拉”遙測監控中心軟體
Taiwan·Risk Class 3·MORTARA INSTRUMENT, INC.·Registered Oct 27, 2011 – Oct 27, 2021CancelledRegistration details
- Analysis ID
- 1a9afaa3d4822ff39dcb49a3daf0eabc
- Customs Code
- DHA00602290604
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 Medicine Science
- Product Type (Level 2)
- E.1025 Arrhythmia Detectors and Alerts
- Import Information
- import
Dates and status
- Registration Date
- Oct 27, 2011
- Expiry Date
- Oct 27, 2021
- Cancellation Date
- Sep 08, 2023
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Motorola" telemetry monitoring center software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 1a9afaa3d4822ff39dcb49a3daf0eabc and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
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