Duns Number:080935429
Device Description: Non-occlusive Gauze Strip Overwrap,3% Bismuth Tribromophenate in Oil Emulsion
Catalog Number
8884437201
Brand Name
Xeroform
Version/Model Number
8884437201
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
-
Product Code
FRO
Product Code Name
Dressing, wound, drug
Public Device Record Key
3e2e3adb-bf13-421d-9f0c-dda0af2592d2
Public Version Date
June 19, 2020
Public Version Number
4
DI Record Publish Date
June 27, 2018
Package DI Number
40884527014980
Quantity per Package
200
Contains DI Package
10884527014989
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 | 672 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1692 |
| U | Unclassified | 17 |