enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Silicone gel sheeting - Wikipedia

    en.wikipedia.org/wiki/Silicone_gel_sheeting

    The exact mechanism of action of silicone gel sheeting has not been fully studied. Currently, many proposed mechanisms explain the efficacy of such treatment, including the occlusion and hydration effect, increased body surface temperature, polarized electric charge, immunological effects, etc. [9] The occlusion and hydration effect is the most studied mechanism of action.

  3. Dermatologic surgical procedure - Wikipedia

    en.wikipedia.org/wiki/Dermatologic_surgical...

    After dermatologic surgery, the presence of suture materials at the wound site can cause redness and swelling, yet these suture reactions may not necessarily indicate allergy or infection. Other common complications include hypertrophic or keloid scars, bruises, suture marks, and skin color changes, which may be temporary or permanent.

  4. Medical grade silicone - Wikipedia

    en.wikipedia.org/wiki/Medical_grade_silicone

    Medical grade silicones are silicones tested for biocompatibility and are appropriate to be used for medical applications. [1] In the United States, the Food and Drug Administration (FDA) Center for Devices and Radiological Health (CDRH) regulates devices implanted into the body. It does not regulate materials other than certain dental materials.

  5. IEC 62366 - Wikipedia

    en.wikipedia.org/wiki/IEC_62366

    IEC 62366 is a process-based standard that aims to help manufacturers of medical devices to design for high usability. It does not address clinical decision-making related to use of the device. The standard will replace ISO/IEC 60601-1-6: Medical electrical equipment - Part 1-6: General requirements for safety - Collateral standard: Usability.

  6. Medical Device Regulation Act - Wikipedia

    en.wikipedia.org/wiki/Medical_Device_Regulation_Act

    Classification panels are to determine which devices intended for human use should be subject to the requirements of class I - general controls, class II - performance standards, or class III - premarket approval. Classification panels are to provide notice to the manufacturers and importers of medical devices intended for human use.

  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. Z-plasty - Wikipedia

    en.wikipedia.org/wiki/Z-plasty

    Z-plasty is a versatile plastic surgery technique that is used to improve the functional and cosmetic appearance of scars. It can elongate a contracted scar or rotate the scar tension line. It can elongate a contracted scar or rotate the scar tension line.

  9. Dermabrasion - Wikipedia

    en.wikipedia.org/wiki/Dermabrasion

    Depending on the level of skin removal with dermabrasion, it takes an average of 7–30 days for the skin to fully heal (re-epithelialize). Often, the procedure is performed for deeper acne scarring and deep surgical scars. Dermabrasion is currently rarely practiced and there are very few doctors who are trained and still perform this surgery.