Duns Number:945020902
Catalog Number
-
Brand Name
Regard™
Version/Model Number
OR0849
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 26, 2019
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
OJH
Product Code Name
Orthopedic Tray
Public Device Record Key
4d5c3160-b072-4840-843a-ab338f2c852a
Public Version Date
September 27, 2019
Public Version Number
2
DI Record Publish Date
March 05, 2018
Package DI Number
20326053112915
Quantity per Package
2
Contains DI Package
10326053112918
Package Discontinue Date
September 26, 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 |