Duns Number:878427491
Device Description: Small Bone Awl Standard
Catalog Number
5078
Brand Name
Innomed, Inc.
Version/Model Number
5078
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
-
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
HWJ
Product Code Name
Awl
Public Device Record Key
fe39e065-76d0-417d-b5bc-b77efd127a8a
Public Version Date
June 10, 2022
Public Version Number
4
DI Record Publish Date
February 17, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 2683 |
2 | A medical device with a moderate to high risk that requires special controls. | 14 |