Duns Number:037304144
Device Description: FUTURE HEALTH CARE MOBILECARE STRETCHER WITH PNEUMATIC BACK ADJUSTMENT CLEARLY MARKED HEIG FUTURE HEALTH CARE MOBILECARE STRETCHER WITH PNEUMATIC BACK ADJUSTMENT CLEARLY MARKED HEIGHT ADJUSTMENT PEDALS ON BOTH SIDES FROM 26TO36" HIGH TRENDELENBURG AND REVERSE TRENDELENBURG ADJUSTMENT PEDALS ON BOTH SIDES FOLD DOWN SIDE RAILS, BUILT IN O2 CYLINDER STORAGE, CENTRAL LOCKING CASTERS BRAKE/STEER PEDAL AT EACH CORNER, I.V. POLE & 4T X 24W X 75 L FOAM MATTRESS SURFACE 75L X 29W, 750LB PATIENT WEIGHT CAPACITY.
Catalog Number
7101
Brand Name
PERSONAL TRANSPORT STRETCHER
Version/Model Number
7101
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FPO
Product Code Name
Stretcher, Wheeled
Public Device Record Key
4b448068-7014-42b8-a0c0-a135e669edf2
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
November 10, 2016
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 | 287 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 10 |