Duns Number:005146311
Device Description: 3-Port Manifold with Check Valves
Catalog Number
2C9282
Brand Name
NA
Version/Model Number
2C9282
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
K932512,K932512
Product Code
FMG
Product Code Name
Stopcock, i.V. Set
Public Device Record Key
2a472f13-69ec-47e5-87df-921e1f472c20
Public Version Date
April 07, 2021
Public Version Number
5
DI Record Publish Date
September 24, 2016
Package DI Number
50085412036866
Quantity per Package
48
Contains DI Package
00085412036861
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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 358 |