Duns Number:020198912
Device Description: HoverMatt Half-Matt 39" W x 45" L
Catalog Number
HM39SPU-HLF-B
Brand Name
N/A
Version/Model Number
HM39SPU-HLF-B
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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"
Yes
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
FRZ
Product Code Name
DEVICE, PATIENT TRANSFER, POWERED
Public Device Record Key
3c05f05a-f165-43e4-97c7-3b2bdada57bf
Public Version Date
April 28, 2022
Public Version Number
2
DI Record Publish Date
July 10, 2019
Package DI Number
57613327487669
Quantity per Package
10
Contains DI Package
07613327487664
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 304 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 1702 |
| U | Unclassified | 12 |