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Dynamic surface tension of saliva: general relationships and application in medical diagnostics. Colloids Surf B Biointerfaces 74(2):457–461. Kotilainen HR, Cyr WH, Truscott W [1992]. Ability of the 1000 mL water leak test for medical gloves to detect gloves with potential for virus penetration.

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FDA regulate latex and nitrile gloves (examination and surgical) as medical devices. Even though the gloves are class 1 device, it requires FDA 510K Clearance, Medical device establishment registration and device listing to market in the USA.Powdered gloves are not allowed to market in the USA for medical purpose.

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Jul 30, 1999·Domestic manufacturers, foreign manufacturers, repackers, or relabelers must list with FDA the type of device they market in the U.S. Also, specifications developers are required to list each type of medical glove if they distribute medical gloves. To list, complete form FDA 2892, "Device Listing," and mail it to the above

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A suspension of sodium hydroxide (34.62 g-0.866 mol, 3.5 eq) in 170 mL of methanol, under mechanical agitation, receives the addition, drop by drop, over the course of 30 minutes, of a solution of ethylamine hydrochloride (70.59 g-0.866 mol, 3.5 eq) in 165 mL of methanol, followed by 1-(3-trifluoromethyl)phenyl-propan-2-one (50 g-0.247 mol).

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Medical gloves are examples of personal protective equipment that are used to protect the wearer and/or the patient from the spread of infection or illness during medical procedures and examinations.