GeneXpert Dx System - XPERT, GENEXPERT DX SYSTEM - CEPHEID

Duns Number:956711444

Device Description: XPERT, GENEXPERT DX SYSTEM

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More Product Details

Catalog Number

900-0523

Brand Name

GeneXpert Dx System

Version/Model Number

GX-I

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K060540,K173263

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

43093d09-cae1-4557-a14e-a07084aead0c

Public Version Date

September 16, 2022

Public Version Number

6

DI Record Publish Date

May 10, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"CEPHEID" Characteristics
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