Taiwan FDA registration 39488d65349b218b6b6caa3c9e42dc87
"Motorola" compression motion test system software
TW: “摩托拉”壓力運動測試系統軟體
Taiwan·Risk Class 2·MORTARA INSTRUMENT, INC.·Registered Jun 16, 2011 – Jun 16, 2016CancelledRegistration details
- Analysis ID
- 39488d65349b218b6b6caa3c9e42dc87
- Customs Code
- DHA00602244800
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.1425 可程式設定之診斷性電腦;; E.2340 心電圖描記器
- Import Information
- import
Dates and status
- Registration Date
- Jun 16, 2011
- Expiry Date
- Jun 16, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Motorola" compression motion test system software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39488d65349b218b6b6caa3c9e42dc87 and manufactured by MORTARA INSTRUMENT, INC.. The authorized representative in Taiwan is WISDOM UNION ENTERPRISE CO., LTD..
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