Duns Number:092364462
Catalog Number
-
Brand Name
Medical Action Industries
Version/Model Number
79554
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 30, 2021
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OHG
Product Code Name
Circumcision tray
Public Device Record Key
072feff5-85dc-49d1-b0a0-0c4b66cffa49
Public Version Date
August 31, 2021
Public Version Number
2
DI Record Publish Date
May 20, 2020
Package DI Number
20809160283957
Quantity per Package
20
Contains DI Package
10809160283950
Package Discontinue Date
August 30, 2021
Package Status
Not in Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 548 |
2 | A medical device with a moderate to high risk that requires special controls. | 2798 |
U | Unclassified | 1 |