Granted Patent B2

US 12,349,869 · App. 16/874,628 · Granted Jul 8, 2025

Inventors: Thomas Bachgaard Jensen (Copenhagen V, DK); Kaspar Mat Matthison-Hansen (Helsingør, DK); Jan Guldberg Hansen (Greve, DK); Troels Nicolaj Qvist (Roskilde, DK); Michael Kappler Hansen (Vallensæk, DK)

Assignee: AMBU A/S

A61B1/0055A61B1/00009A61B1/00045A61B1/00071A61B1/00137A61B1/00165A61B1/005A61B1/0052A61B1/05

Abstract

Claims (27)

1. A medical device operable to obtain images of an internal cavity of a patient, the medical device comprising:

a handle;

a flexible tube having a proximal end adjacent the handle and a distal end, the flexible tube including a first section having a first radial cross-section area and a second section distal of the first section and having a second radial cross-section area smaller than the first radial cross-section area, the second section having a cylindrical outer surface extending along an entire length of the second section;

a bending section extending from the flexible tube and including hinges and segments formed together with the hinges as a single part, the segments comprising a proximal end segment, a distal end segment, and intermediate segments between the proximal end segment and the distal end segment, the segments hingedly connected to each other by the hinges, the proximal end segment including a proximal end segment peripheral wall having an inner surface defining an internal space, the second section positioned at least partly in the internal space, wherein the intermediate segments include outer surfaces, wherein at least some of the outer surfaces of the intermediate sections segments comprise an area profile with a two-dimensional arithmetical mean height parameter, Sa, in the range of 0.9 microns to 9.0 microns as measured by standard ISO 25178;

a tubular sleeve disposed over the bending section; and

a camera assembly supported by the bending section and operable to generate images of distal views,

wherein the at least some of the outer surfaces comprising the Sa in the range of 0.9 microns to 9.0 microns traverse an articulation plane to enable the tubular sleeve to slide on the outer surfaces of the segments, and

wherein the bending section comprises a proximal outer edge surface, and

wherein the tubular sleeve comprises a proximal end with a proximal rim surface facing the proximal outer edge surface.

2. The medical device of claim 1 , wherein the proximal end segment peripheral wall comprises a cavity extending radially outwardly from the inner surface and overlapping the outer surface of the second section, further comprising a hardened adhesive bonded to the outer surface of the second section and extending into the cavity to affix the bending section to the flexible tube.

3. The medical device of claim 1 , wherein the flexible tube further comprises an intermediate section between the first section and the second section, the intermediate section having an intermediate radial cross-section area smaller than the first radial cross-section area and larger than the second radial cross-section area.

4. The medical device of claim 3 , wherein the tubular sleeve is disposed over the bending section and the intermediate section of the flexible tube.

5. The medical device of claim 1 , further comprising a front end cap housing the camera assembly and having a proximal outer surface and a distal outer surface, wherein the distal end segment includes a distal end segment peripheral wall having an inner surface defining an internal space and including a cavity extending radially outwardly from the inner surface, the front end cap positioned at least partly in the internal space of the distal end segment peripheral wall with the cavity overlapping the proximal outer surface, further comprising a second hardened adhesive bonded to the proximal outer surface of the front end cap and extending into the cavity of the distal end segment peripheral wall.

6. The medical device of claim 1 , wherein the Sa is in the range of 1.8 microns to 4.5 microns as measured by the ISO 25178 standard.

7. The medical device of claim 1 , wherein the flexible tube further comprises an intermediate section between the first section and the second section, the intermediate section having an intermediate radial cross-section area smaller than the first radial cross-section area and larger than the second radial cross-section area, wherein the tubular sleeve is disposed over the bending section and the intermediate section of the flexible tube, and wherein the proximal outer edge surface is located between the first section and the intermediate section.

8. The medical device of claim 1 , wherein the proximal end segment comprises a cavity extending radially outwardly from the inner surface, the second section positioned with the cavity overlapping the outer surface of the second section,

the medical device further comprising a hardened adhesive bonded to the outer surface of the second section and extending into the cavity to affix the bending section to the flexible tube, the cavity comprising a through-hole having a closed perimeter.

9. The medical device of claim 8 , wherein the flexible tube comprises a multi-layered structure including a coil and a polymeric layer enclosing the coil, wherein a radial cross-section area of the coil is smaller than the second radial cross-section area, and wherein the outer surface of the second section is formed of the polymeric layer.

10. The medical device of claim 9 , wherein the flexible tube further comprises an intermediate section between the first section and the second section, the intermediate section having an intermediate radial cross-section area smaller than the first radial cross-section area and larger than the second radial cross-section area, wherein the tubular sleeve is disposed over the bending section and the intermediate section of the flexible tube.

11. The medical device of claim 8 , further comprising a front end cap housing an image sensor of the camera assembly and having a proximal outer surface and a distal outer surface with the distal outer edge surface therebetween, wherein the distal end segment includes a distal end segment peripheral wall having an inner surface defining an internal space and including a cavity extending radially outwardly from the inner surface, the front end cap positioned at least partly in the internal space of the distal end segment peripheral wall with the cavity overlapping the proximal outer surface, further comprising a second hardened adhesive bonded to the proximal outer surface of the front end cap and extending into the cavity of the distal end segment peripheral wall.

12. The medical device of claim 1 , wherein the proximal end segment and the distal end segment comprise outer peripheral surfaces with an area profile comprising an Sa of at least 0.9 microns.

13. The medical device of claim 1 , wherein the Sa of the at least some of the outer surfaces of the intermediate segments is at least 2.34+/−0.52 microns.

14. The medical device of claim 1 , wherein the bending section consists essentially of polyoxymethylene.

15. The medical device of claim 14 , wherein the outer surface of the second section of the flexible tube has an Sa greater than 2.34 +/−0.52 microns.

16. The medical device of claim 1 , wherein the bending section consists essentially of polyoxymethylene, and wherein the proximal end segment and the distal end segment comprise outer peripheral surfaces with an area profile comprising an Sa of at least 2.34+/−0.52 microns.

17. The medical device of claim 1 , wherein the proximal end segment peripheral wall comprises through-holes distributed circumferentially and extending from the inner surface through the peripheral wall, wherein each of the through-holes comprises a closed perimeter, the medical device further comprising a hardened adhesive bonded to the outer surface of the second section of the flexible tube and extending into the through-holes of the proximal end segment to affix the bending section to the flexible tube.

18. The medical device of claim 1 , wherein the proximal end segment peripheral wall comprises a plurality of non-overlapping cavities each extending radially outwardly from the inner surface of the proximal end segment and overlapping the outer surface of the second section, further comprising a hardened adhesive bonded to the outer surface of the second section and extending into each of the plurality of non-overlapping cavities to affix the bending section to the flexible tube.

Assignments (2)

Priority Claims (2)

Continuity (3)

References Cited (164)