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  2. Is my medical device approved by Medicare? - AOL

    www.aol.com/lifestyle/medical-device-approved...

    Medicare covers durable medical equipment (DME) a doctor considers medically necessary. Suppliers must be Medicare-approved. There may be out-of-pocket costs.

  3. 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 ...

  4. List of eponymous medical devices - Wikipedia

    en.wikipedia.org/wiki/List_of_eponymous_medical...

    Device Name Specialty Description External link (if no internal link) Adson's forceps: Alfred Washington Adson: General use: Tissue forceps: Adson-Graefe forceps at Whonamedit? [1] ...

  5. Single-use medical devices - Wikipedia

    en.wikipedia.org/wiki/Single-use_medical_devices

    Single-use medical devices include any type of medical equipment, instrument, or apparatus that is disposed of after a single-use in a medical facility. The Food and Drug Administration defines this as any device entitled by its manufacturer that it is intended use is for one single patient and one procedure only. [ 1 ]

  6. Stock up on KN95s after the updated CDC guidelines ... - AOL

    www.aol.com/lifestyle/stock-kn95s-updated-cdc...

    Stock up on KN95s after the updated CDC guidelines: These FDA-approved masks are on sale for $1 a pop at Amazon Devon Kelley,Izabella Zaydenberg August 10, 2021 at 3:00 AM

  7. Pulsed electromagnetic field therapy - Wikipedia

    en.wikipedia.org/wiki/Pulsed_electromagnetic...

    In 2004, a pulsed electromagnetic field system was approved by the FDA as an adjunct to cervical fusion surgery in patients at high risk for non-fusion. [6] On 8/9 September 2020 the FDA recommended to shift PEMF medical devices from the Class 3 category to a Class 2 status. [ 7 ]

  8. Hanger, Inc. - Wikipedia

    en.wikipedia.org/wiki/Hanger,_Inc.

    Hanger, Inc. (formerly Hanger Orthopedic Group, Inc.) is a leading national provider of products and services that assist in enhancing or restoring the physical capabilities of patients with disabilities or injuries that is headquartered in Austin, Texas (formerly Bethesda, Maryland). The company provides orthotic and prosthetic (O&P) services ...

  9. Home medical equipment - Wikipedia

    en.wikipedia.org/wiki/Home_medical_equipment

    Home medical equipment is a category of devices used for patients whose care is being managed from a home or other private facility managed by a nonprofessional caregiver or family member. It is often referred to as "durable" medical equipment (DME) as it is intended to withstand repeated use by non-professionals or the patient, and is ...