Duns Number:001191048
Device Description: Avitene Ultrafoam Collagen Hemostat
Catalog Number
1050030
Brand Name
Avitene Ultrafoam
Version/Model Number
1050030
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
N17600,N17600
Product Code
LMF
Product Code Name
Agent, absorbable hemostatic, collagen based
Public Device Record Key
f54ee5b3-3c83-4c8d-be52-469dbec5af2a
Public Version Date
June 19, 2020
Public Version Number
4
DI Record Publish Date
September 12, 2014
Package DI Number
10801741010535
Quantity per Package
6
Contains DI Package
00801741010538
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CA
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 8 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 348 |
| 3 | A medical device with high risk that requires premarket approval | 18 |