Duns Number:080284658
Device Description: Band Bag 36" X 20" with tape tabs on corners (0120XB) Non-sterile
Catalog Number
-
Brand Name
Sterimed
Version/Model Number
0120XB
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"
Yes
For Single-Use
Yes
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
IZI
Product Code Name
System, X-Ray, Angiographic
Public Device Record Key
3136f538-5546-422b-b4d4-b168ca6eef69
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
March 22, 2017
Package DI Number
10850341007988
Quantity per Package
100
Contains DI Package
00850341007981
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 | 7 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 108 |