Duns Number:884513334
Device Description: Autoimmune EIA ENA Plus Screening test
Catalog Number
96EP
Brand Name
Autoimmune EIA
Version/Model Number
96EP
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
K952253
Product Code
LLL
Product Code Name
EXTRACTABLE ANTINUCLEAR ANTIBODY, ANTIGEN AND CONTROL
Public Device Record Key
fc3eac3b-edc5-4c1e-aac7-c3bfaa66f943
Public Version Date
July 29, 2021
Public Version Number
5
DI Record Publish Date
September 12, 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 | 511 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 428 |
| U | Unclassified | 1 |