The U.S. Food and Drug Administration (FDA EUA) offers emergency use authorizations (EUAs) for unapproved products or new uses for approved items in urgent situations where no suitable alternatives exist. Dozens of companies have sought and received EUAs for their testing kits that screen for SARS-CoV-2 — more commonly referred to as COVID-19 or the novel coronavirus.
The FDA makes a distinction between approved”products and those that got EUAs. It cautions that EUA is not the same as an FDA EUA-cleared or FDA EUA product. However, many media sources — and some distributors and manufacturers of these tests — use the word “approval” or “approved” to discuss FDA EUA testing products that received EUAs.
If you develop any symptoms such as fever, cough and difficulty breathing
Avoid traveling if unnecessary
Electronic Medical Records Software
Revenue Management & Medical Billing System
Surgical gloves are ideal for surgeons and operating room staff that perform procedures where excessive fluids are present causing instruments to become too slick.
Medicare Part B (Medical Insurance) covers blood sugar monitors as durable medical equipment (DME) that your doctor prescribes for use in your home.
FDA EUA Approved, Learn more at www.fda.gov/media/138929/download
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