Taiwan FDA registration 0980fa54351a6952a6bbee0e5a8f7baf
“UPOC＂Fingertip Pulse Oximeter
TW: “怡氧＂指夾式脈搏血氧儀
Taiwan·Risk Class 2·MD·Faciox Inc.·Registered Mar 11, 2023 – Mar 11, 2028ActiveRegistration details
- Analysis ID
- 0980fa54351a6952a6bbee0e5a8f7baf
- License Form
- Ministry of Health Medical Device Manufacturing No. 007825
Company information
- Manufacturer
- Faciox Inc.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Faciox 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
- Mar 11, 2023
- Expiry Date
- Mar 11, 2028
About this record
Access comprehensive regulatory information for “UPOC＂Fingertip Pulse Oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0980fa54351a6952a6bbee0e5a8f7baf and manufactured by Faciox Inc.. The authorized representative in Taiwan is Faciox Inc..
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