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

Radiolucent Armboard

Radiolucent Armboard

ProductID: 800-0297
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.

Provides support during injection of contrast materials; slipping easily under patient’s shoulder.

  • Radiolucent and Phenolic
  • Slide armboard underneath table pad 10" (25 cm) to the desire position
  • 2" (5 cm) Conductive Vinyl Covered Foam Pad (Deluxe or Softcare) sold separately
  • Pad attaches to armboard with adhesive-backed hook & loop fastener
  • 6″W x 36″L (15 cm x 91 cm)

Required Pad: Choose One (sold separately)
2" (5 cm) Deluxe Armboard Pad
2" (5 cm) Softcare Armboard Pad 

Download IFU pdf

Radiolucent Armboard 800-0297

Copyright Notice
All rights reserved. Any duplication, adaption or translation without prior written consent is prohibited unless otherwise provided in relevant copyright laws.

Initial Release: 10/15/17

452 Randolph Street, Abington, MA 02351 USA 
Toll Free
( 888 ) 724-8763  |  Ph (781) 982-7000
(781) 982-7001  |

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

Become familiar with patient positioning device’s features before use with patient. Always practice on a nurse, physician or appropriate volunteer prior to using clinically.

Attaching and Adjusting Armboard to Surgical Table
  1. Place armboard underneath table pad to desire position
Detaching Armboard from Surgical Table
  1. Remove patient from surgical table, then remove armboard underneath table pad
Intended Use
Intended use is to hold patient’s arm. Range of motion is 180°.

General Specifications

Device Dimensions (maximum)
  • Length: 36” +/- 0.5” (91 cm +/- 1 cm)
  • Width: 6” +/- 0.5” (15 cm +/- 1 cm)
  • Depth: .375” +/-  0.5” (.95 cm +/- 1 cm) (without pad)
  • Device Weight: 2 +/-  0.5 lbs. (.09 +/- .22 kg)
  • Single-person installation

Component Overview
RADIOLUCENT ARMBOARD is a surgical table extension that does not attach to side rail.

General Information
  • Product not made with (NRL) Natural Rubber Latex
  • Device supports 500 lb. (227 kg) proportional patient load (6’4” (193 cm) tall patient per 99% human body model)
  • 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)
  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

Maximum load should not exceed appropriate proportion of a patient weighing 500 lbs. (227 kg). Use care with low-maximum load capacity surgical tables that accessory rails are not overloaded. Strictly follow Instructions for Use with your Operating Table system.

Cleaning Recommendation
Follow current Association of periOperative Registered Nurses (AORN) Journal Guidelines for proper cleaning and disinfection procedures.

Follow current Association of periOperative Registered Nurses Journal Guidelines for proper cleaning and disinfection procedures.


Adhere to standards for blood-borne pathogens from the Occupational Safety and Health Administration. Use recommended protective clothing, gloves, masks and eye protection to clean accessory.

Strictly read/follow manufacturer’s directions for cleaning fluids. DO NOT use cleaners containing phenolics.
  1. Remove major contaminants from accessory with disposable materials. Follow appropriate bio-hazard waste disposal procedures.
  2. Apply cleaning fluid liberally to entire accessory and wipe with clean, lint-free cloth until all moisture and cleaning fluid is removed from accessory
  3. Let accessory dry

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-800-0297  REV 3.02

Available Combo Deals