Duns Number:945020902
Catalog Number
-
Brand Name
Regard™
Version/Model Number
OR0902
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 26, 2020
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
-
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
OJH
Product Code Name
Orthopedic Tray
Public Device Record Key
f943fd98-8ee2-484f-a6e4-ef6decb0f872
Public Version Date
August 27, 2020
Public Version Number
4
DI Record Publish Date
March 26, 2018
Package DI Number
20326053113219
Quantity per Package
3
Contains DI Package
10326053113212
Package Discontinue Date
July 01, 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 | 305 |
2 | A medical device with a moderate to high risk that requires special controls. | 558 |