Duns Number:080456871
Device Description: Patient Circuit Kit, Expandable, Adult, Disposable, 3.0 m/120 in
Catalog Number
2066480-026
Brand Name
Vital Signs™
Version/Model Number
2066480-026
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
e70d530e-b9df-4d5c-a529-5c5f553f5665
Public Version Date
October 24, 2022
Public Version Number
2
DI Record Publish Date
July 06, 2021
Package DI Number
50190752108804
Quantity per Package
20
Contains DI Package
10190752108806
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 | 1068 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 780 |
| 3 | A medical device with high risk that requires premarket approval | 65 |
| U | Unclassified | 1 |