Duns Number:867673159
Device Description: Trapeze Base, Brown Vein,1/ea
Catalog Number
-
Brand Name
Drive
Version/Model Number
13017BV
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
IKX
Product Code Name
AID, TRANSFER
Public Device Record Key
7b9cb393-85cd-42de-84f1-49d97ee2a094
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
May 19, 2017
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 3783 |
2 | A medical device with a moderate to high risk that requires special controls. | 832 |