Medical Device Excise Tax definition

Medical Device Excise Tax means the taxes imposed upon the sale of medical devices as defined under Internal Revenue Code Section 4191, which was enacted by the Health Care and Education Reconciliation Act of 2010.
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Medical Device Excise Tax has the meaning set forth in Section 4191 of the Code.
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Examples of Medical Device Excise Tax in a sentence

  • For more information on regulations relating to the medical devices excise tax, see CRS Report R42971, The Medical Device Excise Tax: A Legal Overview, by Andrew Nolan and Internal Revenue Service, “Medical Device Excise Tax: Frequently Asked Questions,” at http://www.irs.gov/uac/Medical-Device-Excise-Tax:-Frequently-Asked-Questions.

  • An extensive discussion of the tax and regulations including the retail exemption, see CRS Report R42971, The Medical Device Excise Tax: A Legal Overview, by Andrew Nolan.

  • Rutter, Understanding the Medical Device Excise Tax (MDET), Slideshow, PriceWaterhouseCoopers.

  • Events Subsequent to Reporting Date200,000 options to acquire fully paid ordinary shares for $0.26 per share expired unexercised.

  • These categories are also included in Effects of the Medical Device Excise Tax on the Federal Tax Liability of the Medical Device Industry, Ernst and Young (Prepared on Behalf of the Advanced Medical Technology Association), November 2012, at http://advamed.org/res.download/14.

  • To the extent we do not comply with the requirements of the Medical Device Excise Tax we may be subject to penalties.

  • This issue is discussed in detail in CRS Report R42971, The Medical Device Excise Tax: A Legal Overview, by (continued...) of the goods, the final point of manufacture may not be clear (for example, in the assembly of kits, which is addressed in the regulations).

  • Michael Ramlet, Robert Book, and Han Zhong ,The Economic Impact of the Medical Device Excise Tax, American (continued...)The F-R study projects job losses of around 43,000.

  • The Medical Device Excise Tax (MDET), a component of the Patient Protection and Affordable Care Act, (known commonly as Obamacare) went into effect after December 31, 2012.

  • A sample was sent for HPLC-MS/ELSD analysis at 2 weeks and at the end of the study.

Related to Medical Device Excise Tax

  • medical device means any instrument, apparatus, appliance, software, implant, reagent, material or other article intended by the manufacturer to be used, alone or in combination, for human beings for one or more of the following specific medical purposes:

  • in vitro diagnostic medical device means any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information:

  • Dental laboratory means a person, firm or corporation

  • Consumables and medical devices means (consumables) items that require regular replacement (e.g. batteries) to keep a medical device (such as a hearing aid) operational. Many medical devices require consumables.

  • Chemical dependency means the physiological and psychological addiction to a controlled drug or substance, or to alcohol. Dependence upon tobacco, nicotine, caffeine or eating disorders are not included in this definition.

  • Licensed health care professional means a person who possesses a professional medical license that is valid in Oregon. Examples include, but are not limited to, a registered nurse (RN), nurse practitioner (NP), licensed practical nurse (LPN), medical doctor (MD), osteopathic physician (DO), respiratory therapist (RT), physical therapist (PT), physician assistant (PA), or occupational therapist (OT).

  • Collaborative drug therapy management means participation by an authorized pharmacist and a physician in the management of drug therapy pursuant to a written community practice protocol or a written hospital practice protocol.

  • Health carrier or "carrier" means a disability insurer

  • Drug therapy management means the review of a drug therapy regimen of a patient by one or more pharmacists for the purpose of evaluating and rendering advice to one or more practitioners regarding adjustment of the regimen.

  • Clinical laboratory means a facility for the microbiological, serological, chemical, hematological, radiobioassay, cytological, immunohematological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of a disease or assessment of a medical condition.

  • Chemical dependency professional means a person certified as a chemical dependency professional by the department of health under chapter 18.205 RCW.

  • Medical evaluation means the process of assessing an individual's health status that includes a medical history and a physical examination of an individual conducted by a licensed medical practitioner operating within the scope of his license.

  • Licensed clinical social worker means an individual who meets the licensed clinical social worker requirements established in KRS 335.100.

  • Licensed health care provider means a physician, physician assistant, chiropractor, advanced registered nurse practitioner, nurse, physical therapist, or athletic trainer licensed by a board.

  • Participating Clinical Laboratory means a Clinical Laboratory which has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Medical cannabis dispensary means an organization issued a

  • Health Canada means the department of the Canadian Government known as Health Canada and includes, among other relevant branches, the Therapeutic Products Directorate and the Health Products and Food Branch Inspectorate;

  • Drug addiction means a disease characterized by a

  • EMA means the European Medicines Agency or any successor agency thereto.

  • Medical Reimbursement Programs means a collective reference to the Medicare, Medicaid and TRICARE programs and any other health care program operated by or financed in whole or in part by any foreign or domestic federal, state or local government.

  • Health screening means the use of one or more diagnostic tools to test a person for the presence or precursors of a particular disease.

  • Occupational therapy means services provided by a qualified occupational therapist, and includes:

  • Licensed health care practitioner means a physician, as defined in Section 1861(r)(1) of the Social Security Act, a registered professional nurse, licensed social worker or other individual who meets requirements prescribed by the Secretary of the Treasury.

  • Medical marijuana dispensary means the location from which a registered cardholder may obtain

  • Participating Clinical Social Worker means a Clinical Social Worker who has a written agreement with the Claim Administrator or another Blue Cross and/or Blue Shield Plan to provide services to you at the time services are rendered.

  • Allowable emissions means the emission rate of a stationary source calculated using both the maximum rated capacity of the source, unless the source is subject to federally enforceable limits which restrict the operating rate or hours of operation, and the most stringent of the following: