Duns Number:945020902
Catalog Number
-
Brand Name
Regard™
Version/Model Number
GY0485
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
September 19, 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
OJF
Product Code Name
Hysterectomy Kit
Public Device Record Key
958aa93e-9280-4df1-aced-1d3db6ac6f81
Public Version Date
September 20, 2019
Public Version Number
4
DI Record Publish Date
May 18, 2017
Package DI Number
20326053112199
Quantity per Package
3
Contains DI Package
10326053112192
Package Discontinue Date
September 19, 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 |