Abstract: A flow control device for medical liquid including a housing having an inlet and an outlet, and a channel formed in an inner surface of the housing, the channel extending at least partly in axial direction; a rotatable member rotatable in relation to the housing without being axially displaced, the rotatable member having at least two apertures; and a core member arranged inside the rotatable member, fixedly connected to the rotatable member. A helical flow path is formed between the lateral surface of the core member and the inner surface of the rotatable member, the at least two apertures of the rotatable member being in communication with said helical flow path, and wherein each of the apertures debouches into the channel in at least one rotational position of the rotatable member.

Abstract: A catheter assembly includes a catheter having on at least part of its surface a hydrophilic surface layer; a wetting fluid pouch including first and second layers of flexible material joined by a seal to form a sealed closure accommodating the wetting fluid; a receptacle forming a cavity for accommodation of the catheter and the wetting fluid pouch. The wetting fluid pouch is openable by compression of the wetting fluid pouch, thereby enabling the wetting fluid to be discharged into the receptacle. At least one of the first and second layers of the wetting fluid pouch extends beyond the seal of the sealed closure to form an attachment area outside the sealed closure, the wetting fluid pouch is attached to an inner surface of the receptacle, and the attachment being provided solely between the receptacle and the attachment area.

Abstract: A use in a medical device of at least one salt of organic acid(s), and preferably a benzoate or a sorbate, as an antimicrobial agent is disclosed, and in particular for the manufacturing of an antimicrobial coating for a medical device, e.g., hydrophyllic urinary catheters, for the prevention of bacterial infection. The pH of the hydrophilic coating may be controlled to be in the range 4.0-8.0, preferably in the range 5.0-6.0, and preferably to be below 7.0. The pH of the hydrophilic coating could be controlled by means of a pH buffer, and preferably a citrate or phosphate buffer. A salt of organic acid in combination with a pH buffer has proven surprisingly efficient for inhibition of bacterial growth, and for prevention of bacterial infections.

Abstract: A catheter assembly is provided comprising a catheter (3;530;630;730) including a catheter tube (32) and a connector (31;531) arranged in one end of the catheter tube. The catheter is preferably a urinary, hydrophilic catheter. Further, the assembly comprises a catheter receptacle (2;520;620;720) for accommodation of at least the catheter tube, wherein the receptacle is provided with an opening (22;622;722), said opening being connected to and closed by the connector (31;531) of the catheter. A method for producing such a catheter assembly is also provided.

Abstract: The invention relates to a method for modification of a biocompatible component comprising the steps of a) providing a biocompatible component at least partly covered by metallic oxide; and b) treating at least a part of said component, which part is covered by said metallic oxide, with an aqueous composition comprising oxalic acid; whereby a modified metallic oxide is obtained. The invention also relates to a biocompatible component comprising a substrate having a surface comprising a) a microstructure comprising pits separated by plateus and/or ridges; and b) a primary nanostructure being superimposed on said microstructure, said primary nanostructure comprising depressions arranged in a wave-like formation.

Abstract: The present invention is based on that local administration of lithium ions in bone tissue has been found to improve the bone formation and bone mass upon implantation of a bone tissue implant in said bone tissue. In particular, the invention relates to a bone tissue implant having an implant surface covered by an oxide layer comprising lithium ions and a method for the manufacture thereof. A blasting powder comprising lithium ions, a method for locally increasing bone formation, and the use of lithium ions or a salt thereof for manufacturing a pharmaceutical composition for locally increasing bone formation are also provided by the present invention.

Abstract: A catheter and catheter assembly are disclosed comprising a urinary catheter comprising an insertion end, a rearward end, and a one way check valve arrangement. The check valve arrangement comprises a tubular part of a flexible material, connected to the rearward end of the catheter and extending past the rearward end in a direction opposite to the insertion end, thereby substantially limiting the flow through the catheter to a single direction from the insertion end to the rearward end. Hereby, a very effective anti-reflux function is achieved, and at the same time the construction is relatively simple and inexpensive, and does not require any essential modifications of the other parts of the urinary catheter.

Abstract: A catheter assembly includes a catheter, preferably having a hydrophilic surface coating; and a package accommodating said catheter. The package preferably also accommodates a wetting fluid. The package includes a first and a second sheet material connected around the edges; a perforation line extending along a non-closed loop in one of said sheet materials, which defines a flap opening; a third sheet material connected by means of an adhesive over said flap opening. The third sheet material with a margin covers the entire flap opening. The adhesive is adapted to maintain a sterile closure of the package before use, and to be resealable after use. The third sheet material forms a tab not provided with adhesive and the tab provides a grip portion for peel opening of the package.

Abstract: There is disclosed a catheter assembly comprising a catheter and a receptacle. The receptacle has an elongate pocket, for accommodating at least an insertable end of said catheter, a urine collection bag, having a width extension wider than a greatest width of said elongate pocket, and at least two tab areas on at least one tab are arranged at the periphery of the urine collection bag on opposite sides of said bag. Further, in a storage state, said elongate pocket is folded over said urine collection bag, and lateral parts of said urine collection bag extending outside said elongate pocket are folded towards each other over said elongate pocket, said lateral parts being dimensioned to overlap each other in the folded disposition, and wherein said tab areas are arranged on said lateral parts and are attached to each other, in at least one point of attachment, to releasably maintain said catheter assembly in a folded disposition during storage.

Abstract: Disclosed is a production method for medical devices with a hydrophilic coating, which ensures adequate adhesion to the substrate, as well as good water retention and low friction properties. Specifically, the method comprises providing a coating solution comprising a hydrophilic polymer to a surface of a substrate to form a non-cross-linked hydrophilic coating; and irradiating the coated substrate, thereby cross-linking the hydrophilic coating and simultaneously sterilizing the medical device. Hereby, a non-cross linked hydrophilic coating is first obtained which is not fit for use as a catheter coating. However, after the step of irradiating the coated substrate, the hydrophilic coating becomes cross-linked, and fit for use e.g. on a urinary catheter. Further, since one and the same irradiation step is used to effect both cross-linking and sterilization, the production can be made more efficient, using fewer production steps and with a shortened production time.

Abstract: The invention relates to a method for modification of a biocompatible component comprising the steps of a) providing a biocompatible component at least partly covered by metallic oxide; and b) treating at least a part of said component, which part is covered by said metallic oxide, with an aqueous composition comprising oxalic acid; whereby a modified metallic oxide is obtained. The invention also relates to a biocompatible component comprising a substrate having a surface comprising a) a microstructure comprising pits separated by plateus and/or ridges; and b) a primary nanostructure being superimposed on said microstructure, said primary nanostructure comprising depressions arranged in a wave-like formation.

Abstract: A self-tapping implant includes a shaft including a coronal end, an apical end, an outer surface having a first axial section and a second axial section, and a self-tapping configuration at the first axial section. The first axial section may be located coronally of the second axial section. Each of the first and second axial sections may include a series of peaks being axially spaced apart by troughs. In addition, the axial spacing between the adjacent peaks in the first axial section may be different than the axial spacing between adjacent peaks in the second axial section. A coronal end portion of the shaft may include the first axial section of the outer surface, and an apical end portion of the shaft may include the second axial section of the outer surface.

Abstract: The present invention is based on that local administration of lithium ions in bone tissue has been found to improve the bone formation and bone mass upon implantation of a bone tissue implant in said bone tissue. In particular, the invention relates to a bone tissue implant having an implant surface covered by an oxide layer comprising lithium ions and a method for the manufacture thereof. A blasting powder comprising lithium ions, a method for locally increasing bone formation, and the use of lithium ions or a salt thereof for manufacturing a pharmaceutical composition for locally increasing bone formation are also provided by the present invention.

Abstract: The present invention is based on that local administration of strontium ions in bone tissue has been found to improve the bone formation and bone mass upon implantation of a bone tissue implant in said bone tissue. In particular, the invention relates to a bone tissue implant having an implant surface covered by an oxide layer comprising strontium ions and a method for the manufacture thereof. A blasting powder comprising strontium ions, a method for locally increasing bone formation, and the use of strontium ions or a salt thereof for manufacturing a pharmaceutical composition for locally increasing bone formation are also provided by the present invention.

Abstract: The present invention relates to a method of providing a patient-specific dental fixture-mating arrangement, such as a dental abutment. According to the method, an arrangement is provided which can only be arranged in one rotational position with respect to a fixture in the jawbone of a patient. The arrangement is designed based on the orientation and inclination of the fixture relative to the jawbone. The invention also relates to a dental implant arrangement, comprising a dental fixture and a final dental restoration having mating indexing means.

Abstract: Implant (10) having a shaft which is adapted in use to be embedded in bone tissue and which has an outer surface provided with a circumferentially-oriented roughness. The circumferentially-oriented roughness has first and second axial sections (19, 21) with each section comprising a series of circumferentially-oriented peaks which have a crest and which are axially spaced apart by troughs. The axial spacing (d) between the crests of adjacent peaks in the first axial section (19) is less than the axial spacing (3d) between the crests of adjacent peaks in the second axial section (21). Although the axial spacing between the crests of adjacent peaks in the first and second axial sections of circumferentially-oriented roughness differs, the first and second axial sections of circumferentially-oriented roughness are adapted in use to provide the same or substantially the same pitch.

Abstract: The present invention relates to a dental implant assembly, comprising a fixture for insertion into a jawbone which is provided with a first thread with a first thread start, and a dental component which is not axially symmetrical and which is provided at its apical end with a second thread with a second thread start having a rotational position which is known in relation to the asymmetrical shape of the dental component for engagement with the first thread.