Duns Number:092364462
Catalog Number
-
Brand Name
Medical Action Industries
Version/Model Number
80280
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 07, 2019
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
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
HFX
Product Code Name
CLAMP, CIRCUMCISION
Public Device Record Key
859a9835-7eca-4883-be50-bea13051c69e
Public Version Date
February 12, 2019
Public Version Number
3
DI Record Publish Date
August 20, 2016
Package DI Number
20809160023621
Quantity per Package
20
Contains DI Package
10809160023624
Package Discontinue Date
February 07, 2019
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 |