Duns Number:009299017
Device Description: UNIVERSAL F CIRCUIT
Catalog Number
U040-61
Brand Name
UNIVERSAL F®
Version/Model Number
U040-61
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
-
Product Code
CAI
Product Code Name
Circuit, breathing (w connector, adaptor, y piece)
Public Device Record Key
a9f037e7-f670-4518-b1f6-1799838102b5
Public Version Date
October 24, 2022
Public Version Number
2
DI Record Publish Date
March 23, 2021
Package DI Number
00612649128054
Quantity per Package
30
Contains DI Package
00612649207698
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 717 |
2 | A medical device with a moderate to high risk that requires special controls. | 41 |