Connector cavity assembly for a medical device and manufacturing method
11318320 ยท 2022-05-03
Assignee
Inventors
Cpc classification
B29C2045/169
PERFORMING OPERATIONS; TRANSPORTING
B29C45/14418
PERFORMING OPERATIONS; TRANSPORTING
A61N1/0563
HUMAN NECESSITIES
Y10T29/49208
GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
B29C45/14639
PERFORMING OPERATIONS; TRANSPORTING
A61N1/37229
HUMAN NECESSITIES
International classification
A61N1/05
HUMAN NECESSITIES
B29C45/14
PERFORMING OPERATIONS; TRANSPORTING
A61N1/372
HUMAN NECESSITIES
Abstract
A connector cavity assembly for a medical device, comprising at least one connector cavity comprising a plurality of electrically conductive electrode contacts spaced apart from each other and a plurality of electrically insulating insulation elements, wherein the electrode contacts and the insulation elements are arranged alternatingly; and a connector cavity housing. The connector cavity assembly is characterized in that the at least one connector cavity is removably arranged within the connector cavity housing, wherein the connector cavity housing exerts a pretension on the at least one connector cavity leading to a liquid-tight sealing between the insulation elements and the electrode contacts.
Claims
1. A connector cavity assembly for a medical device, comprising: at least one connector cavity comprising a plurality of electrically conductive electrode contacts spaced apart from each other and a plurality of electrically insulating insulation elements, wherein the electrode contacts and the insulation elements are arranged alternatingly along a longitudinal axis, and a connector cavity housing, wherein the at least one connector cavity is removably arranged within the connector cavity housing, wherein the connector cavity housing is dimensioned so that it exerts a pretension directed along the longitudinal axis on the at least one connector cavity leading to a liquid-tight sealing between the insulation elements and the electrode contacts.
2. The connector cavity assembly according to claim 1, wherein the at least one connector cavity extends in a longitudinal direction from a proximal end to a distal end and comprises a proximal end element positioned at the proximal end and a distal end element positioned at the distal end.
3. The connector cavity assembly according to claim 2, wherein the connector cavity housing is in contact with the connector cavity solely via the distal end element and the proximal end element.
4. The connector cavity assembly according to claim 1, wherein the connector cavity assembly further comprises at least two connector cavities that are offset to each other in a longitudinal direction and/or in a transversal direction of the connector cavity housing.
5. The connector cavity assembly according to claim 1, wherein the connector cavity housing comprises at least one receiving portion for receiving a further component of a medical device.
6. The connector cavity assembly according to claim 5, wherein the at least one receiving portion enables an attachment of a further component of a medical device by a latching connection.
7. The connector cavity assembly according to claim 1, wherein the connector cavity assembly further comprises at least one of an antenna, a coil, and guideways for an external wiring.
8. The connector cavity assembly according to claim 1, wherein the connector cavity housing comprises at least one spacer on its lower side that is intended to face a body portion of a medical device when the connector cavity housing is part of a medical device.
9. A medical device comprising a connector cavity assembly according to claim 1.
10. The medical device according to claim 9, wherein the connector cavity assembly is embedded into a resin, wherein a connecting port is formed in the resin so that an interior of the at least one connector cavity of the connector cavity assembly is accessible from outside the medical device.
11. The medical device according to claim 9, wherein the medical device is an implantable cardiac pacemaker, an implantable cardioverter defibrillator, or an implantable neurostimulator.
12. A method for manufacturing a connector cavity assembly, comprising the following steps: a) providing a connector cavity housing, b1) assembling a connector cavity by alternatingly placing electrically conductive electrode contacts and electrically insulating insulation elements into a tensioning device or tool, or b2) placing a pre-assembled connector cavity comprising alternatingly positioned electrically conductive electrode contacts and electrically insulating insulation elements into a tensioning device or tool, c) exerting a pretension on the connector cavity with the tensioning device or tool, d) transferring the pretensioned connector cavity into the connector cavity housing, e) releasing or removing the tensioning device, and f) allowing the connector cavity housing to exert a pretension on the connector cavity.
13. The method according to claim 12, wherein the step of assembling the connector cavity or of placing a pre-assembled connector cavity into the pretensioning device is performed without any mandrel being present in an interior space of the connector cavity.
14. The method according to claim 12, wherein the connector cavity housing is a plastic component made by injection molding.
15. A method for manufacturing a medical device, comprising the following steps: a) providing a connector cavity assembly comprising: at least one connector cavity comprising a plurality of electrically conductive electrode contacts spaced apart from each other and a plurality of electrically insulating insulation elements, wherein the electrode contacts and the insulation elements are arranged alternatingly along a longitudinal axis, and a connector cavity housing, wherein the at least one connector cavity is removably arranged within the connector cavity housing, wherein the connector cavity housing is dimensioned so that it exerts a pretension directed along the longitudinal axis on the at least one connector cavity leading to a liquid-tight sealing between the insulation elements and the electrode contacts, b) placing the connector cavity assembly on a body of a medical device, c) establishing an electrical contact between at least one electrically conductive electrode contact of the connector cavity assembly and an electronics housed in the body of the medical device, and d) casting a hardenable resin around the connector cavity assembly.
Description
DESCRIPTION OF THE DRAWINGS
(1) In the Figures:
(2)
(3)
(4)
(5)
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DETAILED DESCRIPTION
(11)
(12) The insulating elements 4 are compressible. The distal end element 2 and the proximal end element 3 are non-elastic. If a pressure is exerted onto the distal end element 2 and/or the proximal end element 3, the insulating elements 4 are (slightly) compressed and sealingly about the adjacent metal rings 5.
(13) The connector cavity 1 is intended to receive a connector of at least one electrode or lead that is to be inserted into an interior space of the connector cavity 1.
(14) This can be seen from
(15) It is apparent, that an interior space 6 of the connector cavity 1 has sufficient space for housing a connector comprising up to eight electrical contacts (each contact contacting a metal spring 50 of the respective metal ring 5). Thus, the connector cavity 1 is suited to receive a connector of a lead having up to eight electrodes.
(16) It is apparent from the depiction of
(17)
(18) The connector cavity housing 8 comprises two connector cavity receiving portions into which the connector cavities 1 are inserted. Thereby, the connector cavity housing 8 directly contacts the respective distal end elements 2 and proximal end element 3 of the connector cavities 1. In doing so, it exerts a pressure onto the distal end elements 2 and the proximal end elements 3 resulting in a pretension of the insulation elements 4 between the conductive metal rings 5. The exerted pressure and thus the resulting pretension is defined by the spatial dimensions of the connector cavity receiving portion, i.e., the distance between a first end portion contacting the distal end element 2 and a second end portion contacting the proximal end element 3 of the respective connector cavity 1. Since this distance is always the same due to a highly standardized manufacturing method (preferably by injection molding) the exerted pressure and the resulting pretension of the connector cavities 1 is also always the same. Even if a high number of connector cavity assemblies 7 is manufactured, the variance between individual connector cavity assemblies 7 is thus very small.
(19)
(20) In the depictions of
(21)
(22) The holding element 10 enables a pre-assembly of the antenna 11 on the connector cavity housing 8 so as to form part of the connector cavity assembly 7. This facilitates a later assembly of the final medical device since the antenna 11 needs no longer be placed into a resin mold upon embedding the antenna 11 and the connector cavities 1 as well as optionally further electrical elements in a resin.
(23)
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(25) In the embodiment shown in
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(27) By providing these guiding pins 17 it is particularly easy to bring the inductive coil 16 into the correct position on the connector cavity housing 8. Furthermore, the holding clips 18 serve for a tight connection of the inductive coil 16 on the connector cavity housing 8.
(28) It would also be possible to provide holding pins 17 and holding clips 18 without additionally providing a holding element 10 for the antenna 11 and/or without providing guideways for the first wiring ribbons 14 that are all present in the embodiment of
(29) It is furthermore easily apparent that the embodiment shown in
(30)
(31) The header portion 20 comprises two connecting ports 21 through each of which a connector of an electrode can be inserted so as to reach the interior of the respective connector cavity 1. In doing so, an electrical contact between the neurostimulator 19 and a connected electrode (not shown in
(32) It will be apparent to those skilled in the art that numerous modifications and variations of the described examples and embodiments are possible in light of the above teachings of the disclosure. The disclosed examples and embodiments may include some or all of the features disclosed herein. Therefore, it is the intent to cover all such modifications and alternate embodiments as may come within the true scope of this invention, which is to be given the full breadth thereof. Additionally, the disclosure of a range of values is a disclosure of every numerical value within that range, including the end points.