Duns Number:027914535
Device Description: Instrumentation For Clinical Multiplex Test Systems
Catalog Number
10-0020-99
Brand Name
INFINITI® PLUS ANALYZER
Version/Model Number
10-0020-99
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
NSU
Product Code Name
Instrumentation for clinical multiplex test systems
Public Device Record Key
ef372b39-23a5-42cd-82f3-16dff1cbbfae
Public Version Date
September 16, 2022
Public Version Number
2
DI Record Publish Date
October 23, 2019
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 |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 19 |