Duns Number:118447207
Device Description: Aurix Single Pack Kit Single Kit with 010405 Aurix Single Pack Kit Label
Catalog Number
-
Brand Name
Aurix Single Pack Kit
Version/Model Number
AUSP-01
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
BK060007
Product Code
PMQ
Product Code Name
Peripheral Blood Processing Device For Wound Management
Public Device Record Key
58cc2d6d-7e60-4020-8087-4292d059d653
Public Version Date
March 21, 2022
Public Version Number
4
DI Record Publish Date
September 30, 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 | 1 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7 |