MGB Alert® Legionella Pneumophila Probe Mix ASR - 48 Reactions - "MGB Alert® Legionella pneumophila Probe is an - Elitechgroup Mdx LLC

Duns Number:117458512

Device Description: "MGB Alert® Legionella pneumophila Probe is an analyte specific reagent that contains a ch "MGB Alert® Legionella pneumophila Probe is an analyte specific reagent that contains a chemically synthesized DNA oligonucleotide designed to detectthe macrophage infectivity potentiator (mip) gene region of Legionella pneumophila. The mix consists of one probe at 1.44 nmol per vial in a 1X TEbuffer solution. The probe is labeled with 6-carboxyfluorescein and has an excitation wavelength maxima of 496 nm and an emission wavelengthmaxima of 517 nm."

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More Product Details

Catalog Number

M800685

Brand Name

MGB Alert® Legionella Pneumophila Probe Mix ASR - 48 Reactions

Version/Model Number

M800685

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

-

Product Code Details

Product Code

MVU

Product Code Name

Reagents, Specific, Analyte

Device Record Status

Public Device Record Key

65c86e6e-73be-4f89-95ef-57f3fd546d14

Public Version Date

October 15, 2020

Public Version Number

2

DI Record Publish Date

September 09, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ELITECHGROUP MDX LLC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 106
2 A medical device with a moderate to high risk that requires special controls. 3