Duns Number:079375431
Device Description: ON-Q* Pain Relief System, SELECT-A-FLOW*, Bolus, NRFit™ Connector, 400 ml, 2-14 ml/hr + 3 ON-Q* Pain Relief System, SELECT-A-FLOW*, Bolus, NRFit™ Connector, 400 ml, 2-14 ml/hr + 3 ml bolus/20 min
Catalog Number
CB006C-N
Brand Name
AVANOS
Version/Model Number
47057
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Conditional
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
K181360,K181360
Product Code
MEB
Product Code Name
Pump, infusion, elastomeric
Public Device Record Key
442e1e88-5da7-4ac6-8d65-50c0cb919329
Public Version Date
July 13, 2020
Public Version Number
1
DI Record Publish Date
July 03, 2020
Package DI Number
10193494470576
Quantity per Package
5
Contains DI Package
00193494470579
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 269 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 5221 |