Duns Number:106712748
Catalog Number
-
Brand Name
CADD
Version/Model Number
21-7002-24
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"
Yes
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
K843772,K843772
Product Code
FRN
Product Code Name
Pump, infusion
Public Device Record Key
d037aa76-411f-4c27-ba80-278c7bc9de98
Public Version Date
August 17, 2018
Public Version Number
4
DI Record Publish Date
October 13, 2016
Package DI Number
30610586022122
Quantity per Package
12
Contains DI Package
10610586022128
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 686 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 1 |