Abstract: A hemostatic device includes a band for being wrapped around a wrist W, securing means for securing the band in a state where the band is wrapped around the wrist, and an inflation portion disposed on an inner peripheral surface of the band, and that is inflated by injecting gas. The inflation portion has a first layer and a second layer which covers an outer surface of the first layer. The first layer is formed of a material which has a larger gas permeation amount per unit area than a material for forming the second layer. The second layer has gap portions which can expose the outer surface of the first layer outward from the second layer in a state where the inflation portion is inflated.

Abstract: A hemostatic device has a band for being wrapped around a puncture site P of a wrist W, securing means for securing the band in a state where the band is wrapped around the wrist, an inflation portion that interlocks with the band, and that is inflated by injecting gas, and an injection portion that can inject gas into the inflation portion. The injection portion is disposed in the band, and is foldable so as to decrease a space formed inside the injection portion. The hemostatic device can thus inflate an inflation portion without using a separate dedicated instrument, which can prevent a hemostasis-requiring site from being unintentionally compressed more than necessary.

Abstract: A hemostatic device has a band for being wrapped around a puncture site of a wrist, securing means for securing the band in a state where the band is wrapped around the wrist, and an inflation portion that interlocks with the band, and that is inflated by injecting gas. The inflation portion includes a first region which stretches when the gas is injected into the inflation portion, and a second region which is less likely to stretch compared to the first region and which is formed of a rigid material. The second region has a micropore which discharges the gas contained in the inflation portion with the lapse of time, in a state where the inflation portion is inflated.

Abstract: Provided is a treatment method and medical apparatus for preventing an object that becomes a causative agent causing pathogenesis of aspiration pneumonitis from invading a lung The treatment method includes a disposing step of disposing a first instrument, which allows the object that becomes a causative agent of aspiration pneumonitis to move from an esophagus to a stomach and suppresses movement of the object from the stomach to a larynx, in the esophagus and disposing a second instrument, which suppresses the object from invading the lung, in at least the larynx.

Abstract: A resin composition comprising: (a) an aromatic co-polyester comprising terephthalic acid, isophthalic acid and a halogen-free bisphenol; and (b) a halogen-containing aromatic co-polyester containing terephthalic acid, isophthalic acid and, at least in part, a bisphenol bearing a halogen substituent(s) as a comonomer. Molded articles prepared from such a resin composition possess excellent mechanical properties, electrical properties and flame-retardant capabilities.