Duns Number:216344051
Device Description: Absorbent gelling fibrous dressing
Catalog Number
66800563
Brand Name
DURAFIBER 2X45 CTN 5
Version/Model Number
66800563
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
NAC
Product Code Name
Dressing, Wound, Hydrophilic
Public Device Record Key
0865be7a-97a1-4e3d-b9c7-eb640599d75a
Public Version Date
July 22, 2021
Public Version Number
4
DI Record Publish Date
May 15, 2020
Package DI Number
05000223467036
Quantity per Package
5
Contains DI Package
05000223466787
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
carton
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 63 |
2 | A medical device with a moderate to high risk that requires special controls. | 126 |
U | Unclassified | 1 |