Duns Number:050579217
Catalog Number
PRD-04476
Brand Name
Panther Fusion
Version/Model Number
INTERNAL CONTROL-X, 960T, IVD
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
Yes
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
NJR
Product Code Name
Nucleic acid amplification assay system, group b streptococcus, direct specimen test
Public Device Record Key
6eca6d64-7d7b-4900-9752-0f5f7242bf83
Public Version Date
August 07, 2019
Public Version Number
1
DI Record Publish Date
July 30, 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 |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 130 |
2 | A medical device with a moderate to high risk that requires special controls. | 311 |
3 | A medical device with high risk that requires premarket approval | 96 |