Duns Number:023904428
Device Description: Petrolatum Dressing XEROFORM SHEET 1 in x 8 in
Catalog Number
-
Brand Name
McKesson
Version/Model Number
2201
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
FRO
Product Code Name
Dressing, Wound, Drug
Public Device Record Key
ac9272c3-0b45-4c29-84e2-6cbb69463ce3
Public Version Date
June 19, 2020
Public Version Number
2
DI Record Publish Date
April 09, 2019
Package DI Number
00612479193086
Quantity per Package
4
Contains DI Package
00612479193079
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 | 870 |
2 | A medical device with a moderate to high risk that requires special controls. | 422 |
U | Unclassified | 44 |