Taiwan FDA registration fa38b2e7a79455d769c047e58bbdf959
Philips patient monitoring system
TW: “飛利浦”病患監視系統
Taiwan·Risk Class 3·INVIVO CORPORATION·Registered Jul 11, 2011 – Jul 11, 2016CancelledRegistration details
- Analysis ID
- fa38b2e7a79455d769c047e58bbdf959
- Customs Code
- DHA00602246602
Company information
- Manufacturer
- INVIVO CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
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.2300 Cardiac monitor (including cardiac data and heart rate monitor)
- Import Information
- import
Dates and status
- Registration Date
- Jul 11, 2011
- Expiry Date
- Jul 11, 2016
- Cancellation Date
- Apr 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自行鍵入
About this record
Access comprehensive regulatory information for Philips patient monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number fa38b2e7a79455d769c047e58bbdf959 and manufactured by INVIVO CORPORATION. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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