Taiwan FDA registration 84dee1c3006469d5210f2a076eb91dcc
“Aulisa” Multiple Patient Digital Vital Sign Monitoring System
TW: “安麗莎” 中央生理訊號監控系統軟體
Taiwan·Risk Class 2·MD·TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.·Registered May 08, 2022 – May 08, 2027ActiveRegistration details
- Analysis ID
- 84dee1c3006469d5210f2a076eb91dcc
- License Form
- Ministry of Health Medical Device Manufacturing No. 007465
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
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E2300 Cardiac Monitor (incl. Cardiac Counter and Heart Rate Alert)
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- May 08, 2022
- Expiry Date
- May 08, 2027
About this record
Access comprehensive regulatory information for “Aulisa” Multiple Patient Digital Vital Sign 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 84dee1c3006469d5210f2a076eb91dcc 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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