Duns Number:340306351
Device Description: Midwest® Rhino XE
Catalog Number
-
Brand Name
Midwest® Rhino XE
Version/Model Number
760035E
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
MRI safety Status
Labeling does not contain MRI Safety Information
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
EFB
Product Code Name
Handpiece, Air-Powered, Dental
Public Device Record Key
f5294f14-e8fc-4bc7-ae9e-89261a0f83d5
Public Version Date
May 17, 2022
Public Version Number
3
DI Record Publish Date
January 28, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 235 |
2 | A medical device with a moderate to high risk that requires special controls. | 326 |