Duns Number:080935429
Device Description: True content to be populated as part of rebranding
Catalog Number
674669
Brand Name
Kangaroo
Version/Model Number
674669
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
-
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
LZH
Product Code Name
Pump, infusion, enteral
Public Device Record Key
333d7b02-b810-40a2-850f-407e4bf66086
Public Version Date
July 15, 2022
Public Version Number
2
DI Record Publish Date
November 27, 2019
Package DI Number
20884521028255
Quantity per Package
30
Contains DI Package
10884521028258
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CASE
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |