NeuMoDxTM GBS Test Strip - NeuMoDx GBS Test Strip - Neumodx Molecular, Inc.

Duns Number:078667309

Device Description: NeuMoDx GBS Test Strip

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More Product Details

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

Product Characteristics

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 Details

Product Code

NJR

Product Code Name

Nucleic acid amplification assay system, group b streptococcus, direct specimen test

Device Record Status

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

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NEUMODX MOLECULAR, INC." Characteristics
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