Taiwan FDA registration 5f959c4b938c0d04335eefc29d7b5f3d
"Anlisa" physiological signal monitoring system
TW: “安麗莎”生理訊號監控系統
Taiwan·Risk Class 2·TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.·Registered Jul 07, 2019 – Jul 07, 2029ActiveRegistration details
- Analysis ID
- 5f959c4b938c0d04335eefc29d7b5f3d
Company information
- Manufacturer
- TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- J General hospital and personal use equipment;; E Cardiovascular Medical Sciences
- Product Type (Level 2)
- J.2910 Clinical Electronic Instrumentation;; E.2700 Blood saturation meter
- Import Information
- Domestic
Dates and status
- Registration Date
- Jul 07, 2019
- Expiry Date
- Jul 07, 2029
About this record
Access comprehensive regulatory information for "Anlisa" physiological signal monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5f959c4b938c0d04335eefc29d7b5f3d and manufactured by TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.. The authorized representative in Taiwan is TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC..
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