Duns Number:092815364
Device Description: The PREMIERCryptococcal Antigen enzyme immunoassay (EIA) is a screening or a semi-quantita The PREMIERCryptococcal Antigen enzyme immunoassay (EIA) is a screening or a semi-quantitative test system for the detection of capsular polysaccharide antigens of Cryptococcus neoformans in serum and cerebrospinal fluid (CSF).
Catalog Number
602096
Brand Name
PREMIER Cryptococcal Antigen
Version/Model Number
602096
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MDU
Product Code Name
Antigen, Elisa, Cryptococcus
Public Device Record Key
5599aff4-55cd-4f7f-8230-498a20d07ee7
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 23, 2016
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 | 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 |