Duns Number:078667309
Device Description: NeuMoDx GBS Test Strip
Catalog Number
200400
Brand Name
NeuMoDxTM GBS Test Strip
Version/Model Number
200400
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K173725,K173725
Product Code
NJR
Product Code Name
Nucleic acid amplification assay system, group b streptococcus, direct specimen test
Public Device Record Key
bb4a4def-6a0f-4d50-a012-e302e50bc060
Public Version Date
April 11, 2019
Public Version Number
1
DI Record Publish Date
April 03, 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 | 4 |
2 | A medical device with a moderate to high risk that requires special controls. | 2 |