Taiwan FDA registration f6b4115f22a6e146fc3f8d1953d7a208
“Aulisa”Oximeter Module
TW: “安麗莎”血氧模組
Taiwan·Risk Class 2·MD·TAIWAN AULISA MEDICAL DEVICES TECHNOLOGIES, INC.·Registered Jul 16, 2022 – Jul 16, 2027ActiveRegistration details
- Analysis ID
- f6b4115f22a6e146fc3f8d1953d7a208
- License Form
- Ministry of Health Medical Device Manufacturing No. 007660
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
- Jul 16, 2022
- Expiry Date
- Jul 16, 2027
About this record
Access comprehensive regulatory information for “Aulisa”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 f6b4115f22a6e146fc3f8d1953d7a208 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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