Duns Number:236059171
Catalog Number
-
Brand Name
LiquiBand Rapid
Version/Model Number
72014030
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
K183570,K183570,K183570
Product Code
MPN
Product Code Name
Tissue Adhesive For The Topical Approximation Of Skin
Public Device Record Key
5f5b9a5a-d7cb-48fd-9eb6-47605b8c2bba
Public Version Date
September 01, 2020
Public Version Number
1
DI Record Publish Date
August 24, 2020
Package DI Number
05036912001304
Quantity per Package
6
Contains DI Package
05036912001298
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 7 |