Duns Number:511139446
Device Description: Kit containing 8 tools, 1 technical manual and 1 bag to keep everything inside, for patien Kit containing 8 tools, 1 technical manual and 1 bag to keep everything inside, for patient transfer and mobilization
Catalog Number
-
Brand Name
Mobi-tools
Version/Model Number
TMK6800
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"
-
For Single-Use
-
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FMR
Product Code Name
DEVICE, TRANSFER, PATIENT, MANUAL
Public Device Record Key
6bbb77fa-d798-4159-88cd-9f9239801753
Public Version Date
November 26, 2019
Public Version Number
1
DI Record Publish Date
November 18, 2019
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 | 170 |