Duns Number:958758146
Device Description: BABB PRIMOBoot, Bariatric (Navy/Gray), 10/each;BABBW PRIMOBoot w/wedge, Bariatric (Navy/Gr BABB PRIMOBoot, Bariatric (Navy/Gray), 10/each;BABBW PRIMOBoot w/wedge, Bariatric (Navy/Gray), 8/each
Catalog Number
BABB, BABBW
Brand Name
PRIMOBoot, Bariatric (Navy/Gray)
Version/Model Number
BABB
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FMP
Product Code Name
Protector, Skin Pressure
Public Device Record Key
4395f8bc-40c4-458a-983b-59b4af817486
Public Version Date
July 02, 2021
Public Version Number
2
DI Record Publish Date
February 20, 2019
Package DI Number
10810006680031
Quantity per Package
10
Contains DI Package
00810006680034
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 | 208 |