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12 Aug 2011, 1:24 pm by Richard Montes
  The plaintiff alleges that on the day before the murder, Marshall, who had voluntarily admitted himself to defendant SLS Residential Inc.'s substance abuse and mental health facility, received a pass to leave the facility to visit his mother. [read post]
13 Dec 2013, 9:54 am
Smith & Nephew, Inc., No. 1:13 CV 1220, 2013 U.S. [read post]
4 Jan 2011, 7:41 pm
Also, over time, the metal components of an ASR Hip can generate small microscopic particles as they move against each other. [read post]
8 Jul 2011, 8:38 pm by Jeralyn
National Institute on Drug Abuse (NIDA), and ElSohly Laboratories, Inc., the federal government's only licensed source of research-grade cannabis (marijuana) used in therapeutic studies. [read post]
24 Sep 2010, 6:43 am
Medical problems associated with the DePuy ASR Hip System include the component device loosening, component malalignment, fracture, and dislocation. [read post]
20 Jul 2010, 12:59 pm by mcarzima@imediainc.com
In September of 2009, Pfizer Inc. and its subsidiary Pharmacia & Upjohn Company Inc. [read post]
3 Jan 2020, 1:27 pm
MSEI developed a multi‐phase plan to build a system to automate the handling of medical devices during its quality testing process, and Universal won the bid to provide the equipment for the first phase. [read post]
8 Jan 2015, 9:44 am
This will be an odd post for us – a research-heavy discussion that doesn’t cite to drug/medical device case law. [read post]
7 Apr 2014, 10:48 am by Ronald V. Miller, Jr.
 The lawsuits allege product liability, negligence, and failure to warn claims against Zimmer, Inc. and Zimmer Holdings, Inc., the manufacturers. [read post]
5 Feb 2014, 6:30 am by Michael B. Stack
    Program   This year’s conference program has seven major components:   WCRI researchers present findings on medical cost drivers and worker outcomes of care. [read post]
26 May 2011, 8:29 am by Ed Wallis
It occurs when the rubbing of metal-on-metal components releases cobalt and chromium ions into the bloodstream. [read post]
10 May 2011, 7:52 pm
The FDA on May 6 sent the request to J&J and 20 other device makers, including Biomet Inc., Stryker Corp. and Zimmer Holdings Inc., asking them to conduct postmarket surveillance of the hip replacements. [read post]