The Biodex Upper Body Cycle is invaluable for upper extremity rehabilitation and conditioning and is wheelchair accessible.
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Upper Body Cycle - a Biodex Informational Video
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M201.2 General Exception
Medical diagnostic equipment shall not be required to comply with one or more applicable requirements in the MDE Standards in the rare circumstances where compliance would alter diagnostically...
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D. Department of Justice Activities Related to Health Care Providers and Medical Equipment
the equipment for transfer; accessible medical equipment (e.g., examination tables and chairs, mammography equipment, weight scales); patient lifts and other methods for transferring individuals...
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M201.2 General Exception (Section-by-Section Analysis)
The MDE NPRM did not propose a general exception for diagnostic equipment that was not capable of meeting the MDE Standards. As described in Section IV.A.1....
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M301.4.2 Clearance Around Base
[See subsections ...]
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1. General Exception
, and would prevent the use of the equipment for its intended diagnostic purpose....
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C. M303 Diagnostic Equipment Used by Patients Seated in a Wheelchair
M303 contains the technical requirements for diagnostic equipment used by patients seated in wheelchairs....
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DEFINITIONS
assistive listening systems; telephones compatible with hearing aids; closed caption decoders; open and closed captioning, including real-time captioning; voice, text, and video-based telecommunications...
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M301.4 Lift Compatibility (Section-by-Section Analysis)
This provision clearly states that diagnostic equipment shall comply with clearance in base or clearance around base....
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PART 3: ACCESSIBLE EXAMINATION ROOMS
These features allow the patient to enter the examination room, move around in the room, and utilize the accessible equipment provided....
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Chapter 3: Technical Requirements
[See subsections ...]
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Chapter 1: Application and Administration
[See subsections ...]
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Wheelchair Space
Space for a single wheelchair and its occupant.
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M101.4 Equivalent Facilitation
The use of alternative designs or technologies that result in substantially equivalent or greater accessibility and usability than specified in the MDE Standards is permitted.
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I. Executive Summary
[See subsections ...]
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M102.2 Undefined Terms (Section-by-Section Analysis)
The MDE NPRM proposed that the meaning of terms not defined in proposed M102.1 or in regulations or policies issued by an enforcing authority, be defined by collegiate dictionaries...
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D.2. - Must requiring officials consider all the Access Board’s technical provisions and functional performance criteria each time they purchase EIT?
No. Requiring officials need only consider all applicable technical provisions from the Access Board’s standards to ensure acquired products provide comparable access (see section...
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Chapter M3: Technical Criteria
[See subsections ...]
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M101.3 Equivalent Facilitation
The use of alternative designs or technologies that result in substantially equivalent or greater accessibility and usability than specified in the standards is permitted.
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Chapter M1: Application and Administration
[See subsections ...]
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Executive Order 13563 (Improving Regulation and Regulatory Review) and Executive Order 12866 (Regulatory Planning and Review): Preliminary Regulatory Assessment
The Office of Management and Budget has reviewed this proposed rule in accordance with Executive Orders 13563 and 12866. Among other things, Executive Order 13563 directs agencies to...
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6. Regulatory Analyses
[See subsections ...]
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5.2.2 Transfer Surface Size Recommendations for M302
5.2.2 Transfer Surface Size Recommendations for M302 Description: The transfer surface is the part of the diagnostic equipment onto which patients who use mobility devices or aids transfer...
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M301.2.4 Unobstructed Transfer (Section-by-Section Analysis)
Specifically, the Access Board asked whether equipment parts should be permitted to extend a maximum of three inches horizontally beyond the edge of the transfer sides, provided they do...