ImmunoCard STAT! EHEC - ImmunoCard STAT! EHEC is an immunochromatographic - MERIDIAN BIOSCIENCE, INC.

Duns Number:092815364

Device Description: ImmunoCard STAT! EHEC is an immunochromatographic rapid test for the qualitative detection ImmunoCard STAT! EHEC is an immunochromatographic rapid test for the qualitative detection of Shiga toxins 1 and 2 (also called Verotoxins) produced by E. coli in cultures derived from clinical stool specimens. ImmunoCard STAT! EHEC is used in conjunction with the patient’s clinical symptoms and other laboratory tests to aid in the diagnosis of diseases caused by enterohemorrhagic E. coli (EHEC) infections.

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More Product Details

Catalog Number

751630

Brand Name

ImmunoCard STAT! EHEC

Version/Model Number

751630

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

K062546

Product Code Details

Product Code

GMZ

Product Code Name

Antigens, All Types, Escherichia Coli

Device Record Status

Public Device Record Key

14a92675-1b47-4c05-81ea-03ee3bca1038

Public Version Date

November 29, 2019

Public Version Number

1

DI Record Publish Date

November 21, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MERIDIAN BIOSCIENCE, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 149
2 A medical device with a moderate to high risk that requires special controls. 46
3 A medical device with high risk that requires premarket approval 1