Duns Number:956711444
Catalog Number
900-0503
Brand Name
GeneXpert Infinity-80 System
Version/Model Number
INFINITY 80-80
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 03, 2022
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OOI
Product Code Name
Real Time Nucleic Acid Amplification System
Public Device Record Key
333a7409-8915-491e-9f13-6c6046cfc82c
Public Version Date
September 16, 2022
Public Version Number
5
DI Record Publish Date
September 12, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 53 |
2 | A medical device with a moderate to high risk that requires special controls. | 78 |