29" KNEE GATCH STRETCHER, MANUAL FOWLER, W/PUSH HANDLES - NO PAD - MOBILECARE STRETCHER. TWENTY NINE INCH BED - M.A.C. MEDICAL INC.

Duns Number:188660844

Device Description: MOBILECARE STRETCHER. TWENTY NINE INCH BED SURFACE. CLEARLY MARKED HEIGHT ADJUST PEDALS MOBILECARE STRETCHER. TWENTY NINE INCH BED SURFACE. CLEARLY MARKED HEIGHT ADJUST PEDALS ON BOTH SIDES WITH RANGE OF 23" TO 36". TRENDELENBURG AND REVERSE TRENDELEBURG 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 WEIGHT CAPACITY 550LB. KNEE GATCH, MANUAL FOWLER, WITH PUSH HANDLES. NO PAD INCLUDED

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More Product Details

Catalog Number

PT1000-29-K-MF-PH-NP

Brand Name

29" KNEE GATCH STRETCHER, MANUAL FOWLER, W/PUSH HANDLES - NO PAD

Version/Model Number

PT1000-29-K-MF-PH-NP

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

Product Characteristics

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 Details

Product Code

FPO

Product Code Name

Stretcher, Wheeled

Device Record Status

Public Device Record Key

f037061c-a103-44e4-9e46-f6b3f3730b33

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

July 26, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"M.A.C. MEDICAL INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 456
2 A medical device with a moderate to high risk that requires special controls. 32