Sec. 20153.
(1) As used in this section:
(a) "Health care provider" means a health facility or agency or a health professional that utilizes single-use devices in furnishing medical or surgical treatment or care to human patients.
(b) "Health professional" means an individual licensed, certified, or authorized to engage in a health profession under article 15, but not including dentists, dental hygienists, or dental assistants under part 166 or veterinarians or veterinary technicians under part 188.
(c) "Original device" means a new, unused single-use device.
(d) "Reprocessed" means with respect to a single-use device, an original device that has previously been used on a human patient and has been subjected to additional processing and manufacturing for the purpose of additional use on a different human patient. Reprocessed includes the subsequent processing and manufacture of a reprocessed single-use device and any single-use device that meets the definition in this subdivision without regard to any description of the device used by the manufacturer of the device or other persons, including a description that uses the term "recycled", "refurbished", or "reused" rather than the term "reprocessed". Reprocessed does not include a disposable or single-use device that has been opened but not used on a person.
(e) "Single-use device" means a medical device that is intended for 1 use or procedure on a human patient, including any device marked "single-use device".
(2) Except as otherwise provided in this section, a health care provider shall not knowingly reuse, recycle, refurbish for reuse, or provide for reuse a single-use device.
(3) This section does not apply to a health care provider that does any of the following:
(a) Utilizes, recycles or reprocesses for utilization, or provides for utilization a single-use device that has been reprocessed by an entity that is registered as a reprocessor and is regulated by the United States food and drug administration.
(b) Utilizes an opened, but unused single-use device for which the sterility has been breached or compromised and that meets all of the following requirements:
(i) The single-use device has not been used on a human patient and has not been in contact with blood or bodily fluids.
(ii) The single-use device has been resterilized.
(c) Utilizes a used single-use device on the same human patient in an emergency situation.
(4) A health care provider that violates this section is guilty of a felony punishable by imprisonment for not more than 10 years or a fine of not more than $50,000.00, or both. A violation of this section by a health professional is considered a violation of article 15 and that health professional is subject to administrative action under sections 16221(h) and 16226.
History: Add. 2010, Act 25, Imd. Eff. Mar. 26, 2010 Popular Name: Act 368
Structure Michigan Compiled Laws
Act 368 of 1978 - Public Health Code (333.1101 - 333.25211)
Article 17 - Facilities and Agencies (333.20101...333.22260)
368-1978-17-201 - Part 201 General Provisions (333.20101...333.20211)
Section 333.20101 - Meanings of Words and Phrases; Principles of Construction.
Section 333.20102 - Definitions; A.
Section 333.20104 - Definitions; C to G.
Section 333.20106 - Definitions; H.
Section 333.20108 - Definitions; I to N.
Section 333.20109 - Definitions; N to S.
Section 333.20121-333.20127 - Repealed. 2022, Act 187, Imd. Eff. July 25, 2022.
Section 333.20144 - Licensing on Basis of Approved Building Program.
Section 333.20151 - Cooperation; Professional Advice and Consultation.
Section 333.20155a - Repealed. 2022, Act 187, Imd. Eff. July 25, 2022.
Section 333.20158 - Biannual Inspection Reports for Certain Entities.
Section 333.20169 - HIV Infected Test Subject; Compliance With Reporting Requirements; Definitions.
Section 333.20170 - Medical Records Access; Compliance.
Section 333.20172 - Policies and Procedures; Publication and Distribution.
Section 333.20173 - Repealed. 2006, Act 28, Eff. Apr. 1, 2006.
Section 333.20174 - Practice Agreement; Designation of Physician by Health Facility or Agency.
Section 333.20176a - Health Facility or Agency; Prohibited Conduct; Violation; Fine.
Section 333.20182 - Abortion; Objection; Participation in Medical Procedures Not Required; Immunity.
Section 333.20183 - Abortion; Refusal to Give Advice; Refusal to Participate In; Immunity.
Section 333.20188 - Repealed. 2004, Act 119, Eff. Nov. 27, 2005.
Section 333.20189a - Written Practice Agreement; Condition of Employment; Prohibited.
Section 333.20192 - Do-Not-Resuscitate Order; Execution Not Required.
Section 333.20193 - Compliance.
Section 333.20197 - Human Cloning in Facility Owned or Operated by Health Facility or Agency.
Section 333.20199 - Violations; Penalties.
Section 333.20202 - Responsibilities of Patient or Resident.
Section 333.20203 - Guidelines; Immunity; Other Remedies at Law Neither Expanded nor Diminished.
Section 333.20211 - Repealed. 2022, Act 187, Imd. Eff. July 25, 2022.