Taiwan FDA registration 80d1a47468a9c3af4b6a94fee1164dfb
“Wistron Medical” IntelliBridge Enterprise (Non-Sterile)
TW: “緯創醫學” 醫療資料界接整合系統(未滅菌)
Taiwan·Risk Class 1·MD·WISTRON MEDICAL TECHNOLOGY CORPORATION·Registered Aug 28, 2018 – Aug 28, 2023ExpiredRegistration details
- Analysis ID
- 80d1a47468a9c3af4b6a94fee1164dfb
- License Form
- Ministry of Health Medical Device Manufacturing No. 007405
Company information
- Manufacturer
- WISTRON MEDICAL TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- WISTRON MEDICAL TECHNOLOGY CORPORATION
Product details
- Intended Use
- The main function of this software system is to convert the patient's physiological parameters (such as heartbeat, pulse, blood pressure, respiration rate, blood oxygen concentration, etc.) to the computer system through the physiological monitor, and use the connection authorization as the main information service, which can perform the communication, data correspondence, message transmission, and data transmission and exchange between the Wistron Medical software system and the hospital system, the following blank.
- Product Type (Level 1)
- P Devices for radiology
- Product Type (Level 2)
- P9999 Other
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 28, 2018
- Expiry Date
- Aug 28, 2023
About this record
Access comprehensive regulatory information for “Wistron Medical” IntelliBridge Enterprise (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 80d1a47468a9c3af4b6a94fee1164dfb and manufactured by WISTRON MEDICAL TECHNOLOGY CORPORATION. The authorized representative in Taiwan is WISTRON MEDICAL TECHNOLOGY CORPORATION.
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