M301 provides technical criteria for diagnostic equipment used by patients in a supine, prone, or sidelying position, and M302 provides technical criteria for diagnostic equipment used by...
Search Results "CPE: Customer Premises Equipment"
Commonly Searched Documents
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M301 Diagnostic Equipment Used by Patients in Supine, Prone, or Side-Lying Position; M302 Diagnostic Equipment Used by Patients in Seated Position
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Machinery Spaces (§203.5)
Machinery Spaces (§203.5) Spaces used only by service personnel for maintenance, repair, or occasional monitoring of equipment Examples: elevator pits/ penthouses, mechanical/...
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M302.3.2 Leg Supports (Section-by-Section Analysis)
The MDE NPRM did not propose to require stirrups to provide a method of supporting, positioning, and securing the patient’s legs for diagnostic equipment used by patients in the seated position...
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M301.3.2 Leg Supports
Where stirrups are provided, leg supports shall also be provided and shall comply with M305.4.
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M301.3.2 Stirrups
Where stirrups are provided, they shall provide a method of supporting, positioning, and securing the patient’s legs.
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M305.2.2 Length (Section-by-Section Analysis)
specifically sought public input with question 19, asking if the proposed length of the transfer supports would be sufficient to facilitate transfer and maintain position on the diagnostic equipment...
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5.1.1 Transfer Surface Height Adjustability Recommendation for M301 and M302
The adjustability of medical diagnostic equipment will facilitate transfers for all types of patient populations by providing the ability to “pair” the transfer surface of diagnostic equipment...
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5.4.3 Transfer Support Height for M301 and M302
used by patients in a supine, prone, or side-lying position, and diagnostic equipment used by patients in a seated position....
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5.4.5 Transfer Support Position Recommendation for M301 and M302
It addresses angled supports or contoured portions of horizontal supports often provided for ergonomics or equipment design considerations....
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M305.2.1 Location (Section-by-Section Analysis)
While the MDE Advisory Committee recommended separate requirements based on the type of diagnostic equipment, stretchers and imaging equipment, the Access Board believes that the type of...
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M305.2.7 Clearance (Section-by-Section Analysis)
Specifically, the Access Board sought input from the public in question 22, on whether transfer supports on diagnostic equipment could provide 1½ inches minimum clearance around the gripping...
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Healthcare Stories - Fred Nisen Part 1 of 6
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Healthcare Stories - Michael Grice
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HEALTHCARE STORIES - Elizabeth Grigsby Part 3 of 3
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Healthcare Stories - Mary Delgado
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Healthcare Stories - Dianne Collins
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HEALTHCARE STORIES - DENISE SHERER JACOBSON Part 1 of 4
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Healthcare Stories - Jim LeBrecht
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Healthcare Stories - Frances Deloatch
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Healthcare Stories - Jennifer Thomas Part 1 of 2
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M307.2 Tactilely Discernible
Operable parts shall be tactilely discernible without activation.
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§ 1194.23(h)
(h) Where a telecommunications product delivers output by an audio transducer which is normally held up to the ear, a means for effective magnetic wireless coupling to hearing...
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B. Regulatory Flexibility Act
The Regulatory Flexibility Act (RFA) requires federal agencies to analyze the impact of regulatory actions on small entities, unless an agency certifies that the rule will not have a...
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M307.2 Tactilely Discernible (Section-by-Section Analysis)
The MDE NPRM proposed that operable parts intended for patient use be tactilely discernible without activation. Patients who are blind or have low vision have difficulty...
