Duns Number:117174678
Catalog Number
-
Brand Name
Regard™
Version/Model Number
NU00263N
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 31, 2020
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
-
Product Code
OJG
Product Code Name
Neurological Tray
Public Device Record Key
3607fd52-b3d2-4c24-96a0-f4c86c8eefb7
Public Version Date
August 31, 2020
Public Version Number
3
DI Record Publish Date
November 21, 2019
Package DI Number
20194717100246
Quantity per Package
1
Contains DI Package
10194717100249
Package Discontinue Date
August 31, 2020
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 | 589 |
2 | A medical device with a moderate to high risk that requires special controls. | 961 |