Helix Elite™ Molecular Standards: Inactivated Standard - Helix Elite™ Molecular Standards Inactivated - MICROBIOLOGICS INC.

Duns Number:060467826

Device Description: Helix Elite™ Molecular Standards Inactivated Chlamydia trachomatis/ Neisseria gonorrhoeae Helix Elite™ Molecular Standards Inactivated Chlamydia trachomatis/ Neisseria gonorrhoeae (CT/NG)

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More Product Details

Catalog Number

HE0045N

Brand Name

Helix Elite™ Molecular Standards: Inactivated Standard

Version/Model Number

HE0045N

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)

-

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

OHQ

Product Code Name

Multi-analyte controls unassayed

Device Record Status

Public Device Record Key

0b4415d4-a02e-412b-b14c-6131e15dfff0

Public Version Date

December 21, 2020

Public Version Number

2

DI Record Publish Date

April 30, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MICROBIOLOGICS INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1104
2 A medical device with a moderate to high risk that requires special controls. 24