Taiwan FDA registration d61178c52e694a925dcc7823e0903dba
Philips Integrated Medical Data Convergence System (Unsterilized)
TW: “飛利浦”醫療資料界接整合系統 (未滅菌)
Taiwan·Risk Class 1·PHILIPS MEDICAL SYSTEMS·Registered Jan 28, 2014 – Jan 28, 2024ExpiredRegistration details
- Analysis ID
- d61178c52e694a925dcc7823e0903dba
- Customs Code
- DHA09401382108
Company information
- Manufacturer
- PHILIPS MEDICAL SYSTEMS
- Manufacturer Country
- United States
- Authorized Representative
- PHILIPS TAIWAN LIMITED
Product details
- Intended Use
- This software and the connection license as the main information service, can perform the communication between information, data correspondence, message transmission, data conversion, as well as the data transmission and exchange between Philips products and hospital systems, the following blanks.
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.2010 Medical image storage devices;; P.2020 Medical imaging communication devices
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Jan 28, 2014
- Expiry Date
- Jan 28, 2024
About this record
Access comprehensive regulatory information for Philips Integrated Medical Data Convergence System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d61178c52e694a925dcc7823e0903dba and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.
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