Abstract: A medical assembly, preferably a sterilized one, includes a medical article (5) and a package containing the article, the package including a hollow support element (2) inside which the article (5) is free, a first protective element (3), called a stopper, which can be coupled to the support element (2) of the article, such that the support element (2) has a grip part (20) that protrudes from the stopper (3), and a second hollow protective element (4), called a cover. The cover can be coupled to the stopper (3) in such a way as to delimit, in cooperation with the stopper (3), a chamber (8) inside which there extends the grip part (20) of the support element, and, in the state when the cover is coupled to the stopper, a part of the stopper (3) protrudes from the cover (4).

Abstract: A package for an object includes a support element with means for coupling the object to the support element. A first hollow protective element is provided as a stopper coupled to the support element of the object. The support element presents a grip portion which projects from the stopper, the support element, alone or in co-operation with the stopper, defining a first chamber containing the object. A second hollow protective element is provided as a cover. The cover is coupled to the stopper so as to cooperate with the stopper to define a second chamber inside which the grip portion of the support element extends. The cover is coupled to the stopper, with the grip portion of the stopper projecting from the cover. The means for coupling is configured to hold the object suspended through the means for coupling, so that the object extends into the space left free between the means for coupling and a bottom portion of the support element.

Abstract: The invention relates to a method for surface treatment of a biocompatible metal material, such as an implant, which comprises the following consecutive steps: i) abrasive mechanical treatment of the surface of said material using abrasive calcium phosphate grains, such as a mixture of hydroxyapatite and tricalcium phosphate; ii) acid treatment by hot dipping of said material in a bath comprising sulphuric acid and hydrochloric acid, followed by at least one rinse with demineralised water; iii) sodic treatment by hot dipping of said material in a soda bath followed by at least one rinse with demineralised water and drying in hot air. The implant thus treated has a surface with increased roughness with a triple level of porosity (macro-, micro- and nano-porosity) as well as improved hydrophilic properties. The method can be used for implants made of titanium alloys, such as the TA6V ELI alloy.

Abstract: A package for an object includes a support element with a coupler configured to hold the object captive in a given orientation of the object, and release the object by pivoting the object. The support element alone defines a first chamber containing the object, the support element also includes at least two parts that can be coupled and uncoupled relative to each other by inter-fitting with partial overlap, so as to form the first chamber containing the object. A stopper is coupled to the support element of the object by inter-fitting with partial overlap such that the support element presents a grip portion that projects from the stopper. A cover is coupled to the stopper by inter-fitting with partial overlap so as to cooperate with the stopper to define a second chamber inside which the grip portion of the support element extends, and while the cover is coupled to the stopper, a grip portion of the stopper projects from the cover.

Abstract: A package for an object includes a support element with means for coupling the object to the support element. A first hollow protective element is provided as a stopper coupled to the support element of the object. The support element presents a grip portion which projects from the stopper, the support element, alone or in co-operation with the stopper, defining a first chamber containing the object. A second hollow protective element is provided as a cover. The cover is coupled to the stopper so as to cooperate with the stopper to define a second chamber inside which the grip portion of the support element extends. The cover is coupled to the stopper, with the grip portion of the stopper projecting from the cover.

Abstract: A packaging element (2, 3) has two shells (21, 22, 31, 32), each shell having a margin (210, 220) defining an access opening giving access to the inside of the shell, said packaging element (2, 3) having at least a “closed” configuration in which the shells form a chamber that is substantially closed and that is suitable for receiving an article, such as a medical implant. The packaging element (2, 3) further has a sealing strip (4) that extends, outside the shells (21, 22, 31, 32), over the entire length of the margins (210, 220) of the shells of the packaging element, and from one margin (210, 220) of the shell to the other margin (220, 210) of the shell in such a manner as to seal the chamber defined by the two shells. An assembly has two packaging elements received one inside the other, with a corresponding sealing method.

Abstract: A package for an object includes a support element with means for coupling the object to the support element. A first hollow protective element is provided as a stopper coupled to the support element of the object. The support element presents a grip portion which projects from the stopper, the support element, alone or in co-operation with the stopper, defining a first chamber containing the object. A second hollow protective element is provided as a cover. The cover is coupled to the stopper so as to cooperate with the stopper to define a second chamber inside which the grip portion of the support element extends. The cover is coupled to the stopper, with the grip portion of the stopper projecting from the cover.

Abstract: A package for an object such as a preferably-sterile medical component, includes: a support element provided with elements for coupling the object; a stopper that can be coupled to the support element in such a manner as to define a first chamber for containing the object, and such that a grip portion of the support element projects from the stopper; and a cover that can be coupled to the stopper in such a manner as to define a second chamber inside which the grip portion of the support element extends, and such that a portion of the stopper coupled to the support element projects from the cover.

Abstract: A package (1) for an object such as a preferably-sterile medical component, includes: a support element (2) provided with elements (21) for coupling the object (5); a stopper (3) that can be coupled to the support element (2) in such a manner as to define a first chamber (7) for containing the object (5), and such that a grip portion (20) of the support element (2) projects from the stopper (3); and a cover (4) that can be coupled to the stopper (3) in such a manner as to define a second chamber (8) inside which the grip portion (20) of the support element (2) extends, and such that a portion (30) of the stopper (3) coupled to the support element (2) projects from the cover (4).

Abstract: A medical assembly, preferably a sterilized one, includes a medical article (5) and a package containing the article, the package including a hollow support element (2) inside which the article (5) is free, a first protective element (3), called a stopper, which can be coupled to the support element (2) of the article, such that the support element (2) has a grip part (20) that protrudes from the stopper (3), and a second hollow protective element (4), called a cover. The cover can be coupled to the stopper (3) in such a way as to delimit, in cooperation with the stopper (3), a chamber (8) inside which there extends the grip part (20) of the support element, and, in the state when the cover is coupled to the stopper, a part of the stopper (3) protrudes from the cover (4).

Abstract: A package (1) for an object such as a preferably-sterile medical component, includes: a support element (2) provided with elements (21) for coupling the object (5); a stopper (3) that can be coupled to the support element (2) in such a manner as to define a first chamber (7) for containing the object (5), and such that a grip portion (20) of the support element (2) projects from the stopper (3); and a cover (4) that can be coupled to the stopper (3) in such a manner as to define a second chamber (8) inside which the grip portion (20) of the support element (2) extends, and such that a portion (30) of the stopper (3) coupled to the support element (2) projects from the cover (4).

Abstract: The invention concerns a method for preparing macro-porous synthetic ceramics designed in particular for bone substitution. The invention also concerns macro-porous synthetic ceramics comprising pores of controlled dimensions, distributed in number and in surface in a predetermined manner, the interconnection between the pores thereof being controlled.