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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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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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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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
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Chapter 1: Application and Administration
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Wheelchair Space
Space for a single wheelchair and its occupant.
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Do companies need to review all their products and services for accessibility and usability?
Do companies need to review all their products and services for accessibility and usability? Yes. Accessibility and usability must be assessed for individual products and...
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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
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§ 1194.23(g)
(g) If the telecommunications product allows a user to adjust the receive volume, a function shall be provided to automatically reset the volume to the default level after every use.
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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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§ 1194.23(b)
(b) Telecommunications products which include voice communication functionality shall support all commonly used cross-manufacturer non-proprietary standard TTY signal protocols.
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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
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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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Section 1193.2 Scoping (Section-by-Section Analysis)
Bell Atlantic and NYNEX were concerned that appropriately equipped telecommunications equipment and customer premises equipment should be available to implement or complement their services...
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M101.4 Equivalent Facilitation (Section-by-Section Analysis)
Therefore, the only change to this provision was to adjust the section number to allow for the addition of the new provision, M101.3 Existing Diagnostic Equipment....
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M304 Diagnostic Equipment Used by Patients in Standing Position
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