Duns Number:060467826
Device Description: Helix Elite™ Molecular Standards Inactivated Macrolide and Quinolone-Resistant Mycoplasma Helix Elite™ Molecular Standards Inactivated Macrolide and Quinolone-Resistant Mycoplasma Genitalium
Catalog Number
HE0069N
Brand Name
Helix Elite™ Molecular Standards: Inactivated Standard
Version/Model Number
HE0069N
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
OHQ
Product Code Name
Multi-Analyte Controls Unassayed
Public Device Record Key
2692ff41-1d77-49aa-a64a-0def1fa22342
Public Version Date
February 24, 2022
Public Version Number
1
DI Record Publish Date
February 16, 2022
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
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 |