Taiwan FDA registration 5113025f1d41dcd32b8c1fec717f23a9
“Aulisa＂Infant Oximeter Module
TW: “安麗莎＂嬰兒血氧模組
Taiwan·Risk Class 2·MD·TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.·Registered Apr 03, 2022 – Apr 03, 2027ActiveRegistration details
- Analysis ID
- 5113025f1d41dcd32b8c1fec717f23a9
- License Form
- Ministry of Health Medical Device Manufacturing No. 007452
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)
- E2700 Oximeter
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Apr 03, 2022
- Expiry Date
- Apr 03, 2027
About this record
Access comprehensive regulatory information for “Aulisa＂Infant Oximeter Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5113025f1d41dcd32b8c1fec717f23a9 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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