Duns Number:831375089
Device Description: Cohesive Bandage, Non-Sterile, 2" x 5" Stretched, Tan, Latex
Catalog Number
8972
Brand Name
PremierPro
Version/Model Number
8972
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)
Yes
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
FQM
Product Code Name
Bandage, Elastic
Public Device Record Key
92f47bd8-2b11-4edb-92c9-c180ad139171
Public Version Date
May 25, 2022
Public Version Number
2
DI Record Publish Date
August 29, 2020
Package DI Number
10818566016789
Quantity per Package
36
Contains DI Package
00818566016782
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 | 486 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 177 |
| U | Unclassified | 1 |