Device for preparing a medical sensor for use
First Claim
1. A device for storing and calibrating a medical sensor while preventing contamination thereof, said medical sensor including a needle portion, comprising:
- a container open at one end, said container including a first chamber capable of holding a first calibrating fluid;
a stopper sized to fit in said open end of said container, said stopper having an opening therethrough to receive the medical sensor, and sized so that the medical sensor can be moved rotatably and perpendicularly in relation to said stopper while a fluid-tight seal between said stopper and said medical sensor is maintained; and
an elastomeric material formed into a wall that defines a second chamber within said container, proximate said stopper and said open end of the container, said second chamber being capable of holding a second calibrating fluid, said wall separating the first and second calibrating fluids and being flexible and puncturable by the needle portion of the medical sensor, for self-sealing around said needle portion and resealing after said needle portion is withdrawn.
2 Assignments
0 Petitions
Accused Products
Abstract
The apparatus includes a container (26) having an open upper end into which is fitted a stopper (20). From the lower peripheral surface of the stopper (20) depends a membrane (24) which forms a chamber containing one calibrating fluid (28). The stopper (20) is adapted to permit a medical probe to extend therethrough, the hub (16) needle (14) and sensor (12) of which extend beneath the membrane (24). Another calibrating fluid (30) is located in the container (26) beneath the membrane (24). The membrane (24) is capable of maintaining a fluid-tight seal as it is punctured by the needle (14) and of re-sealing itself when the needle (14) is removed, without permitting contamination of the one calibrating fluid (28) by the other calibrating fluid (30) and vice versa.
30 Citations
13 Claims
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1. A device for storing and calibrating a medical sensor while preventing contamination thereof, said medical sensor including a needle portion, comprising:
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a container open at one end, said container including a first chamber capable of holding a first calibrating fluid; a stopper sized to fit in said open end of said container, said stopper having an opening therethrough to receive the medical sensor, and sized so that the medical sensor can be moved rotatably and perpendicularly in relation to said stopper while a fluid-tight seal between said stopper and said medical sensor is maintained; and an elastomeric material formed into a wall that defines a second chamber within said container, proximate said stopper and said open end of the container, said second chamber being capable of holding a second calibrating fluid, said wall separating the first and second calibrating fluids and being flexible and puncturable by the needle portion of the medical sensor, for self-sealing around said needle portion and resealing after said needle portion is withdrawn. - View Dependent Claims (2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12)
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13. A device for storing and calibrating a medical sensor while preventing contamination thereof, comprising:
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a container having an open end, said container being divided into a first chamber capable of receiving a first calibrating fluid and a second chamber capable of receiving a second calibrating fluid, said second chamber being removable from the container through the open end; a stopper sized to fit said open end of the container and including an opening in which the medical sensor can be retained when stored within the second chamber; and an elastomeric membrane sealingly separating said first chamber from said second chamber, said elastomeric membrane being characterized by its ability to seal around the medical sensor when perforated thereby, as the medical sensor is advanced from the second around the medical sensor when perforated thereby, as the medical sensor is advanced from the second chamber into the first chamber, and its ability to reseal when the medical sensor is withdrawn from the first chamber, thereby preventing mixing of the first and second calibrating fluids.
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Specification