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UMHS Specimen to Charge Code Rapid Finder List 2011-2025 free printable template

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UMPS DEPARTMENT OF PATHOLOGY: Specimen To Charge Code Rapid Finder List 88304 88305 88304 88302 88305 88304 88305 88304 88304 88304 88307 88305 88307 88305 88309 88307 88305 88305 88302 88304 88304 88304 88302 88304 88304 88305 88307 88304 88307 88305 88304 88305 88305 88307 88304 88305 88309 88307 88304 88307 88307 88305 88304 88307 88305 88305 88309 88305 88307 88305 88307 88305 88305 88307 88305 88307 88307 88309Abortioninduced Abortion
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To maintain patient safety standards, specimens must be properly labeled with the name of the patient, a numerical identifier that is unique to the patient (like DOB or SSN), collection date, and the source of the specimen, where applicable.
The label must contain the following legible information: Patient name. Patient medical record number, with check digit. Patient location.
The specimen label must contain the patient's name, medical record number, and identity of the tissue.
Surgical procedures that remove human tissue become surgical pathology specimens. These specimens are examined by physicians, called pathologists, who specialize in the gross and microscopic examination of these tissues.
Urines, faeces and sputum samples, aspirates: refrigerate within one hour.

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UMHS Specimen to Charge Code Rapid Finder is a tool used to quickly match laboratory specimens with their corresponding charge codes within the University of Michigan Health System (UMHS).
Healthcare professionals and laboratory personnel who handle specimens and process billing within UMHS are required to file the UMHS Specimen to Charge Code Rapid Finder.
To fill out the UMHS Specimen to Charge Code Rapid Finder, users should input the specimen details and select the appropriate charge codes associated with the tested specimens, following the guidelines provided by UMHS.
The purpose of the UMHS Specimen to Charge Code Rapid Finder is to streamline the billing process by ensuring accurate mapping of specimens to their respective charge codes, thus enhancing efficiency and reducing billing errors.
Information that must be reported includes the specimen type, the associated tests, the charge codes, and any relevant patient details necessary for accurate processing and billing.
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