Duns Number:945020902
Catalog Number
-
Brand Name
Regard™
Version/Model Number
GS0174
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 27, 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
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
GCX
Product Code Name
Apparatus, Suction, Operating-Room, Wall Vacuum Powered
Public Device Record Key
d6f523df-19be-4a51-8914-2b5f48e053be
Public Version Date
August 28, 2020
Public Version Number
3
DI Record Publish Date
December 16, 2016
Package DI Number
20326053103234
Quantity per Package
10
Contains DI Package
10326053103237
Package Discontinue Date
August 27, 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 | 305 |
2 | A medical device with a moderate to high risk that requires special controls. | 558 |