Duns Number:080950957
Catalog Number
-
Brand Name
Regard™
Version/Model Number
NU1086
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
789d56b2-823f-4849-858e-a3eac2025057
Public Version Date
August 22, 2019
Public Version Number
1
DI Record Publish Date
August 14, 2019
Package DI Number
20326053117156
Quantity per Package
16
Contains DI Package
10326053117159
Package Discontinue Date
-
Package Status
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 | 305 |
2 | A medical device with a moderate to high risk that requires special controls. | 558 |