A biocompatible material for bone repair is described. The bone repair composition includes a mixture of a type I collagen, a type I collagen-glycosaminoglycan coprecipitate, tricalcium phosphate; and bioactive glass. Methods of using the composition for bone repair, and a kit for the bone repair composition are also described.

Methods for processing tissue are provided. In some embodiments, the methods comprise methods for decellularizing tissue samples by applying high hydrostatic pressure to the tissues samples. In some embodiments, the methods comprise methods for thawing tissue samples and/or reducing the bioburden in a sample by applying high hydrostatic pressure to the tissue samples.

The invention relates to a biocompatible molded part for supporting new bone formation, in particular the reformation of a jaw bone or a jaw bone portion in a mammal, preferably a human, wherein the molded part is suitable to be placed on the jaw bone and is designed as a solid body. The invention also relates to a composition for producing a biocompatible molded part, a method for producing a biocompatible molded part, a use of a biocompatible molded part and a kit comprising a plurality of molded parts.

The present invention relates to a sterilized medical dressing for treating wounds comprised of a polymer sponge containing an antimicrobial agent and a silicon adhesive secured to the dressing surface. The dressing can be exposed initially to gamma radiation and later sterilized by ethylene oxide or alternatively it can be sterilized by ethylene oxide and later irradiated by gamma radiation. z The sponge dressing can also contain at least one biofilm reducing agent, at least one chelating agent and an ionic and non-ionic surfactant.

The present invention relates to a wound healing PVA sponge dressing using negative capillary pressure of the dressing material together with auxiliary negative pressure for wound treatment. The PVA sponge dressing is pretreated with gram positive and gram negative biocidal dyes for insertion into or over a wound. A negative pressure pump is mounted to the PVA sponge dressing to produce additional capillary pressure for withdrawing fluid or water vapor from the sponge dressing and a cover is mounted over the sponge material and negative pressure pump forming a unitary sealed package for placement over a wound.

The present invention relates to a sponge dressing for treating wounds comprised of a polymer sponge containing a plurality of antimicrobial dyes with at least one dye being gram positive and at least one other dye being gram negative and a silicon adhesive secured to a sponge surface. The sponge dressing can be exposed initially to gamma radiation and later sterilized by ethylene oxide or alternatively it can be sterilized by ethylene oxide and later irradiated by gamma radiation. The sponge dressing has a morphology characterized by an average pore throat diameter of 0.5-500 m and a porosity ranging from about 60% to about 99.5%. The sponge dressing can also contain at least one biofilm reducing agent, at least one chelating agent and an ionic and non-ionic surfactant.

The disclosed embodiment relates to an injection device that is a single patient use, disposable device containing a needle and a cartridge containing a drug, pharmaceutical product or other injectable agent. The device is initially provided in a pre-armed state in a first engagement configuration wherein the needle is separated from the septum of a cartridge. To arm the injection device, the professional urges the device from the first engagement or pre-armed configuration to a second engagement or armed configuration wherein the needle pierces the septum and provides a sterile fluid path to the drug, pharmaceutical product or other injectable agent contained within the cartridge. The disclosed embodiment is particularly adaptable to dental anesthetic applications, as well as other medical and veterinary applications.

Method for sterilizing a hydrophilically coated medical device.

An autonomous device for detecting characteristics of a medium to be measured is disclosed. The device includes a sensor, a first microcontroller and a second microcontroller. The first microcontroller has a memory which is not resistant against gamma radiation during the sterilization of the device and the second microcontroller has a memory which is resistant against gamma radiation during the sterilization of the device.

A root canal filling cone made of a material having a composition that can maintain its physical and chemical characteristics and shelf life after sterilization, and a process of sterilizing the point/cone prior to shipment to a user. In one aspect, the cone is made of a composition that includes a plurality of base polymers of substantially equal amounts, and nanoparticles, which can withstand sterilization by gamma irradiation. In one embodiment, the compound includes Gutta Percha based polymers. In another aspect, the Gutta Percha based cone is packaged and sterilized by irradiation prior to shipment to a user. In one embodiment of the present invention, the irradiation is gamma irradiation.