Duns Number:061310132
Catalog Number
-
Brand Name
Streamline Airless System Set with Locksite Needleless Access Sites
Version/Model Number
SL-2010M2096
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 28, 2020
Issuing Agency
In HIBCC
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
FJK
Product Code Name
Set, Tubing, Blood, With And Without Anti-Regurgitation Valve
Public Device Record Key
1fff9fde-f22d-412c-ade0-7f184237d04f
Public Version Date
September 29, 2020
Public Version Number
4
DI Record Publish Date
September 01, 2015
Package DI Number
M535SL2010M20965
Quantity per Package
32
Contains DI Package
M535SL2010M20960
Package Discontinue Date
September 28, 2020
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 167 |