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  2. The main discussion of these abbreviations in the context of drug prescriptions and other medical prescriptions is at List of abbreviations used in medical prescriptions. Some of these abbreviations are best not used, as marked and explained here.

  3. Ohio bioscience sector - Wikipedia

    en.wikipedia.org/wiki/Ohio_bioscience_sector

    The overall economic impact of the bioscience industry in Ohio, including healthcare, amounted to $148.2 billion in 2007, representing 15.7% of Ohio's economic output. [5] Half of the biotech industry is located in northeast Ohio, with 574 firms, while central and southern Ohio are home to around 200 each.

  4. Global Center for Health Innovation - Wikipedia

    en.wikipedia.org/wiki/Global_Center_for_Health...

    The building nearing completion in 2013. The Global Center for Health Innovation, [1] also known as the Medical Mart, was a $465 million joint venture by Cuyahoga County and MMPI to construct a permanent showroom of medical, surgical and hospital goods along with a new Huntington Convention Center of Cleveland in downtown Cleveland, Ohio. [2]

  5. J&J to restructure orthopedic business after medical device ...

    www.aol.com/news/j-j-raises-annual-profit...

    Johnson & Johnson on Tuesday said it has embarked on a two-year restructuring program for its orthopedics business after third-quarter medical devices sales fell short of Wall Street expectations ...

  6. Ethicon - Wikipedia

    en.wikipedia.org/wiki/Ethicon

    Ethicon, Inc., is a subsidiary of Johnson & Johnson.The company is part of the Johnson & Johnson MedTech business segment. It was incorporated as a separate company under the Johnson & Johnson umbrella in 1949 to expand and diversify the Johnson & Johnson product line.

  7. Single use medical device reprocessing - Wikipedia

    en.wikipedia.org/wiki/Single_Use_Medical_Device...

    The practice of reusing medical devices labeled for only one use began in hospitals in the late 1970s. [8] After a thorough review by the U.S. FDA in 1999 and 2000, [8] the agency released a guidance document for reprocessed SUDs that began regulating the sale of these reprocessed devices on the market, [9] under the condition that third-party reprocessors would be treated as the manufacturer ...

  8. ISO 13485 - Wikipedia

    en.wikipedia.org/wiki/ISO_13485

    ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.

  9. Custom-made medical device - Wikipedia

    en.wikipedia.org/wiki/Custom-made_medical_device

    Jurisdiction Definition Legislation Australia A medical device that: (a) is made specifically in accordance with a request by a health professional specifying the design characteristics or construction of the medical device; and (b) is intended: (i) to be used only in relation to a particular individual; or (ii) to be used by the health professional to meet special needs arising in the course ...