Call Customer Service at 781-531-9164 for Pricing and Ordering Information.

Schure Slide, Full-Size

Schure Slide, Full-Size

ProductID: 800-0069
Customer Service
For product pricing and information, please call our Customer Service Team at 781-531-9164 or fill out the Request a Quote form.

The Full-Size Schure Slide enables hospital and operating room personnel to easily slide patient from one bed to another. Each shifter slides easily on the bed sheet or stretcher pad because of its slippery, high-density polyethylene material. The rigid slide bridges the gap between uneven surfaces. Unique design has ten hand holes for easy insertion and removal of slide. Every recovery room or emergency room should have one.

  • Non-disposable, no need to waste red bags
  • Radiolucent and not made with natural rubber latex
  • Reduce back injuries and increase patient comfort
  • Speed-up turnover time – hang Schure Slide in every O.R.
  • Won’t stain – spray and wipe clean
  • 72"L x 22"W x 3/16" (183 cm x 56 cm x .48 cm)

Important! Please note that the Schure Slides are made for sliding a patient from one surface to another and are not constructed to support patient weight.

 


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Schure Slide, Full Size   800-0069

Initial Release: 12/29/2011


Manufacturer
SchureMed 
(081001460)
452 Randolph Street, Abington, MA 02351 USA 
Toll Free
 ( 888 ) 724-8763  |  Ph (781) 982-7000  |  Fax (781) 982-7001  |  orders@schuremed.com


Authorized Representative
Emergo Europe, Prinsessegracht 20, 2514 AP The Hague, The Netherlands

INSTRUCTIONS FOR USE
Become familiar with the features of patient positioning device before use with a patient. Always practice use on a nurse, physician or appropriate volunteer prior to using clinically.

Clean Sheet Transfer

  1. Lock stretcher against procedure table, gently pull draw sheet up, tilting patient up on side. Position Schure Slide under draw sheet, then lower patient down
  2. Using draw sheet, steadily slide patient over Schure Slide to transfer table
  3. Gently remove Schure Slide from beneath patient
Soiled Sheets Transfer
  1. Lock stretcher against procedure table, take a clean draw sheet and wrap it around Schure Slide covering 3/4 of slide bottom
  2. Gently tilt patient up on side, leaving soiled sheets down. Position Schure Slide and clean draw sheet beneath patient, directly under torso
  3. Medic #1 pulls draw sheet, white Medic #2 pushes patient, sliding patient over Schure Slide onto transfer table
  4. Remove Schure Slide from beneath patient
CLEANING INSTRUCTION
  1. Spray and wipe clean with hospital approved disinfectant

INTENDED USE
Intended use if for personnel to effortlessly slide patient from one gurney or table to another, eliminating risk of back injury while increasing patient comfort dramatically. 

GENERAL SPECIFICATIONS
Device Dimensions (maximum)
  • Length: 72” +/- 0.5” (183 cm +/- 1 cm)
  • Width: 22” +/- 0.5” (56 cm +/- 1 cm)
  • Thickness: 3/16” +/- 0.5” (.48 cm +/- 1 cm)
  • Device Weight: 9 +/- 0.5 lbs. (4 +/- .22 kg)
COMPONENT OVERVIEW
Schure Slide enables personnel to easily slide patient from one bed to another.

GENERAL INFORMATION
  • Product not made with (NRL) Natural Rubber Latex
  • Product warranty covers product from manufacturing defects for period of 2 years
  • If damaged in shipping, call Customer Service at (888) 724-8763 or (781) 982-7000 to obtain Return Material Authorization (RMA) number. For product warranty issues, contact Customer Service.
  • Product is maintenance-free, check product condition before next use
  • Life of device is 5 years under normal use
  • Store device between –4°F to +86°F (-20°C to 30°C)
Disposal
  1. General - Prevent infection by cleaning and disinfecting product before disposal
  2. Packaging - Dispose packaging material via household waste according to national requirements
  3. SchureMed accepts back used or retired products - or dispose of product in accordance with national requirements


Product Use Warnings
WARNING! 
Hazard resulting from incorrect use. 

USER NOTICE?Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.
USER NOTICE
Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.


USER NOTICE?Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.
USER NOTICE?Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.
USER NOTICE?Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established.
USER NOTICE?Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the competent authority of the Member State in which the user and/or patient is established

 

 

IFU-800-0069  REV 3.01

Available Combo Deals