Duns Number:152680815
Device Description: Low Volume Tubing Set
Catalog Number
B95-079-2
Brand Name
Lifemed Low Volume Tubing Set
Version/Model Number
B95-079-2
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"
-
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
86923ad7-8e54-4480-a8a1-b286c21376e5
Public Version Date
June 07, 2019
Public Version Number
3
DI Record Publish Date
October 06, 2015
Package DI Number
10852250006052
Quantity per Package
10
Contains DI Package
00852250006055
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 6 |