Taiwan FDA registration f0c63760ca6e51e7886639ed4629e6f1
“Mortara” Ambulatory Telemetry Module
TW: “摩托拉”數位傳輸器
Taiwan·Risk Class 2·MD·MORTARA INSTRUMENT, INC.·Registered Dec 22, 2016 – Dec 22, 2021CancelledRegistration details
- Analysis ID
- f0c63760ca6e51e7886639ed4629e6f1
- License Form
- Ministry of Health Medical Device Import No. 029255
- Customs Code
- DHA05602925504
Company information
- Manufacturer
- MORTARA INSTRUMENT, INC.
- Manufacturer Country
- United States
- Authorized Representative
- WISDOM UNION ENTERPRISE CO., LTD.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2910 Radio Wave Physiological Signal Transmission Receiver
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 22, 2016
- Expiry Date
- Dec 22, 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 “Mortara” Ambulatory Telemetry Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f0c63760ca6e51e7886639ed4629e6f1 and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
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