Taiwan FDA registration d3c3b14bb362fdeabccc85a05b7ef113
“Nonin” Finger Pulse Oximeter
TW: “諾寧”手指型血氧飽和測定儀
Taiwan·Risk Class 2·MD·NONIN MEDICAL, INC.·Registered Aug 14, 2015 – Aug 14, 2020CancelledRegistration details
- Analysis ID
- d3c3b14bb362fdeabccc85a05b7ef113
- License Form
- Ministry of Health Medical Device Import No. 027592
- Customs Code
- DHA05602759202
Company information
- Manufacturer
- NONIN MEDICAL, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BIOSYSTEMS INC.
Product details
- Product Type (Level 1)
- E Cardiovascular devices
- Product Type (Level 2)
- E2700 Oximeter
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 14, 2015
- Expiry Date
- Aug 14, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Nonin” Finger 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 d3c3b14bb362fdeabccc85a05b7ef113 and manufactured by NONIN MEDICAL, INC.. The authorized representative in Taiwan is BIOSYSTEMS INC..
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