Patient interface
US-2020114107-A1 · Apr 16, 2020 · US
US12409289B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12409289-B2 |
| Application number | US-202217668559-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 10, 2022 |
| Priority date | Mar 16, 2015 |
| Publication date | Sep 9, 2025 |
| Grant date | Sep 9, 2025 |
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The present specification is directed a method manufacturing a patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway. The method includes locating a shell, a first sub section of a seal forming structure, and a first section of the seal forming structure in a tool. The first sub section includes a groove. The first section is constructed from a thermoformable material. The method further includes introducing a moulding material to the tool and overmolding the shell, the first sub section, and the first section. The moulded material forms a second sub section of the seal forming structure that connects the first sub section to the shell and fully encloses the first section within the groove.
Opening claim text (preview).
The invention claimed is: 1. Method of manufacturing a patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway, the method comprising: locating a shell, a first sub section of a seal forming structure, and a first section of the seal forming structure in a tool, wherein the first sub section includes a first end with at least one flange and a second end that includes a groove, and wherein the first section is constructed from a thermoformable material; subsequently introducing a moulding material to the tool and overmoulding the shell, the first sub section, and the first section, wherein the moulding material forms a second sub section of the seal forming structure that connects the first sub section to the shell and fully encloses the first section within the groove; and locating the first section in the groove along an insertion axis prior to moulding, wherein the insertion axis does not intersect the at least one flange. 2. The method of claim 1 , further comprising casting or moulding the first section into the groove of the first sub section. 3. The method of claim 1 , further comprising assembling the first section separately from the first sub section. 4. The method of claim 1 , further comprising positioning the shell apart from the first section to form a gap prior to introducing the moulding material. 5. The method of claim 1 , wherein the first sub section and the second sub section are constructed from the same material. 6. The method of claim 5 , wherein the first sub section and the second sub section are constructed from silicone. 7. The method of claim 1 , wherein the first sub section and the second sub section are constructed from different materials, each of which is different than the thermoformable material. 8. The method of claim 1 , wherein the second sub section extends between the first sub section and the shell. 9. The method of claim 1 , wherein the second sub section is partially received within the groove and around the first section. 10. The method of claim 1 , wherein the first sub section includes a sealing flange and a support flange. 11. The method of claim 1 , wherein the shell is formed from a rigid material. 12. The method of claim 1 , wherein after overmoulding, the seal forming structure, the thermoformable material, and the shell are permanently fixed in this one piece construction. 13. A patient interface for treatment of sleep disordered breathing using air pressure by delivery of air to a patient's airway, the patient interface comprising a shell and a seal forming structure, wherein the seal forming structure comprises a first section of a thermoformable material and a second section of another material, wherein the second section comprises different sub sections, wherein a first sub section includes a first end with at least one flange and a second end with a groove, and wherein the first section is located in the groove along an insertion axis by means of a second sub section, the second sub section connecting the seal forming structure to the shell and fully enclosing the first section within the groove, wherein the shell and the second sub section are integrally formed together to form a one piece construction, and wherein the insertion axis intersecting the shell and not intersecting the at least one flange. 14. The patient interface of claim 13 , wherein the at least one flange includes a sealing flange configured to contact the patient and a support flange having a greater thickness than the sealing flange for supporting the sealing flange, and wherein the insertion axis intersects neither the support flange nor the sealing flange. 15. The patient interface of claim 13 , wherein the second sub section extends between the first sub section and the shell. 16. The patient interface of claim 13 , the second sub section is partially received within the groove and around the first section. 17. The patient interface of claim 13 , wherein the second sub section is overmoulded onto the shell. 18. The patient interface of claim 13 , wherein the first sub section and the second sub section are each constructed from a different material than the first section.
Medical equipment; Accessories therefor (bloodbags, medical bags B29L2031/7148; artificial eyes B29L2011/0008) · CPC title
Use of polymers having silicon, with or without sulfur, nitrogen, oxygen, or carbon only, in the main chain, as moulding material · CPC title
by combined operations {or combined techniques}, e.g. welding and stitching · CPC title
by moulding (using a particular moulding technique, see the relevant technique {, e.g. by injection B29C45/14467}) · CPC title
Methods of manufacture, assembly or production · CPC title
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