TWI533844B - Blood analyte meter - Google Patents
Blood analyte meter Download PDFInfo
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- TWI533844B TWI533844B TW102128741A TW102128741A TWI533844B TW I533844 B TWI533844 B TW I533844B TW 102128741 A TW102128741 A TW 102128741A TW 102128741 A TW102128741 A TW 102128741A TW I533844 B TWI533844 B TW I533844B
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- 239000008280 blood Substances 0.000 title claims description 58
- 210000004369 blood Anatomy 0.000 title claims description 58
- 239000012491 analyte Substances 0.000 title claims description 3
- 239000012503 blood component Substances 0.000 claims description 44
- 239000000463 material Substances 0.000 claims description 23
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 239000000306 component Substances 0.000 description 4
- 238000010586 diagram Methods 0.000 description 4
- 238000010295 mobile communication Methods 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 2
- 230000000694 effects Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/75—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated
- G01N21/77—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator
- G01N21/78—Systems in which material is subjected to a chemical reaction, the progress or the result of the reaction being investigated by observing the effect on a chemical indicator producing a change of colour
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
- G01N21/84—Systems specially adapted for particular applications
- G01N21/8483—Investigating reagent band
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N2201/00—Features of devices classified in G01N21/00
- G01N2201/02—Mechanical
- G01N2201/022—Casings
- G01N2201/0221—Portable; cableless; compact; hand-held
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- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Plasma & Fusion (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Molecular Biology (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
- Investigating Or Analysing Biological Materials (AREA)
- Instructional Devices (AREA)
Description
本發明係關於一種血液成份分析儀，特別是一種整合採血裝置與試片於同一本體中的血液成份分析儀。 The invention relates to a blood component analyzer, in particular to a blood component analyzer which integrates a blood collection device and a test piece in the same body.
傳統之血液成份分析儀基本上包含彼此分離之採血裝置與試片。也就是說，使用者需要先讓採血裝置(可能是一採血針)刺破其手指表面後，再把所血液範本滴到試片上。蒐集到血液範本之試片通常會置入一血液成份讀取裝置之插槽，以完成血液範本中特定成份數值的估算。 A conventional blood component analyzer basically comprises a blood collection device and a test piece separated from each other. That is to say, the user needs to first let the blood collection device (probably a blood collection needle) puncture the surface of the finger, and then drop the blood sample onto the test piece. The test strips that collect the blood sample are usually placed in a slot of a blood component reading device to complete the estimation of the specific component values in the blood sample.
除此之外，現有之試片在蒐集完血液範本後的顏色變化即便是透過照相機的影像擷取，可能會因為環境光線的關係，使得所擷取之影像沒辦法精確地反映出血液範本中實際的血液成份數值的狀況。如果再把溫度這個會影響試片色彩顯現的這個變數考慮進去的話，現有的試片影像擷取並不一定能產出接近實際數值的結果。 In addition, the color change of the existing test piece after collecting the blood sample, even through the image of the camera, may be due to the relationship between the ambient light, so that the captured image can not accurately reflect the blood sample. The actual blood component value status. If the temperature, which affects the color appearance of the test piece, is taken into account, the existing test image capture does not necessarily produce results close to the actual value.
本發明揭露之一種血液成份分析儀(blood analyte meter)包含一本體、一採血裝置位於本體內、以及一試片(test strip)同樣位於本體內。本體包含有之不透光之一第一表面與透光之一第二表面，且本體之一第一內表面係設計成可在該本體內部反射經由該第二表面輸入之一光線。 A blood analyte meter disclosed in the present invention comprises a body, a blood collection device located in the body, and a test strip located in the body. The body includes a first surface that is opaque and one of the light transmissive second surfaces, and one of the first inner surfaces of the body is designed to reflect a light input through the second surface inside the body.
本發明是把採血裝置與試片整合在同一個血液成份分析儀 本體/結構中。使用者無需另外把試片插入到血液成份讀取裝置之插槽才可獲得血液成份數值。除此之外，本發明之血液成份分析儀本體的第一表面(舉例來說，本體的上表面)乃是一個不透光的設計，可有效阻絕環境光線對於血糖試片顏色變化之擷取所造成的影響。 The invention integrates the blood collection device and the test piece into the same blood component analyzer In the body / structure. The user does not need to insert the test piece into the slot of the blood component reading device to obtain the blood component value. In addition, the first surface of the body of the blood component analyzer of the present invention (for example, the upper surface of the body) is an opaque design, which can effectively block the environmental light from capturing the color change of the blood glucose test piece. The impact.
再加上，本發明之血液成份分析儀基本上乃是配合行動通訊裝置(如手機)使用。也就是說試片的影像是透過行動通訊裝置上附屬的照相機所擷取，所以當本發明的血液成份分析儀被置放在行動通訊裝置上時只有本體的第二表面是可以讓上述照相機的光線通過，在沒有太多環境光線的干擾下完成試片影像的擷取，以確保數值判斷的精確性。 In addition, the blood component analyzer of the present invention is basically used in conjunction with a mobile communication device such as a mobile phone. That is to say, the image of the test piece is captured by a camera attached to the mobile communication device, so that when the blood component analyzer of the present invention is placed on the mobile communication device, only the second surface of the body can be used for the camera. Light passes through, and the image of the test piece is captured without interference from too much ambient light to ensure the accuracy of the numerical judgment.
100、200、300‧‧‧血液成份分析儀 100, 200, 300‧‧‧ blood component analyzer
102、202、302‧‧‧本體 102, 202, 302‧‧‧ ontology
104、204、304‧‧‧試片 104, 204, 304‧‧‧ test strips
106、206、306‧‧‧採血裝置 106, 206, 306‧‧ ‧ blood collection device
108、208、305‧‧‧第一表面 108, 208, 305‧‧‧ first surface
112、212、322‧‧‧第二表面 112, 212, 322‧‧‧ second surface
113、218、324‧‧‧內部光源 113, 218, 324‧‧‧ internal light source
114、222、326‧‧‧可撓材質層 114, 222, 326‧‧‧ flexible material layer
214、312、316‧‧‧開口 214, 312, 316‧‧
216‧‧‧輸血通道 216‧‧‧transfusion channel
308‧‧‧第一表面之第一預定位置 308‧‧‧ First predetermined position of the first surface
314‧‧‧試片之第一預定位置 314‧‧‧ First predetermined position of the test piece
第1圖是依據本發明一實施例之血液成份分析儀之示意圖；第2圖為依據本發明之一實施例的血液成份分析儀的示意圖；以及第3圖為依據本發明之一實施例的血液成份分析儀的示意圖。 1 is a schematic view of a blood component analyzer according to an embodiment of the present invention; FIG. 2 is a schematic view of a blood component analyzer according to an embodiment of the present invention; and FIG. 3 is a view of an embodiment of the present invention. Schematic diagram of the blood component analyzer.
請參閱第1圖，第1圖是依據本發明一實施例之血液成份分析儀100之示意圖。血液成份分析儀100包含一本體102、一試片104位於本體102內、以及一採血裝置106同樣位於本體102內。本體102另外包含有一第一表面108與一第二表面112。第一表面108上之一第一預定位置係可被設計來讓採血裝置106被啟動時突出於本體102之外，以與使用者之手指有所接觸。第一表面108之一第二預定位置可有一開口105的設置，使得當使用者之手指跟採血裝置106接觸後得以讓血液範本能夠透過開口105為試片104所 蒐集。 Please refer to FIG. 1. FIG. 1 is a schematic diagram of a blood component analyzer 100 according to an embodiment of the present invention. The blood component analyzer 100 includes a body 102, a test strip 104 located within the body 102, and a blood collection device 106 located within the body 102. The body 102 further includes a first surface 108 and a second surface 112. One of the first predetermined positions on the first surface 108 can be designed to protrude beyond the body 102 when the blood collection device 106 is activated to contact the user's fingers. The second predetermined position of one of the first surfaces 108 may have an opening 105 such that when the user's finger contacts the blood collection device 106, the blood sample can be passed through the opening 105 as the test piece 104. collect.
當試片104蒐集到血液範本時，試片104會有顏色上的變化。而此試片104的顏色，當使用手機之螢幕光源照射或是手機之附設之照相機發出之光線照射時，較不容易受到環境光的影響，使得經由試片104的顏色而判斷所蒐集到的血液範本中之血液成份數值能夠較為精確。而為了有效阻絕環境光的影響，第一表面108係設計為一不透光之表面而第二表面112則可是可透光之表面。因為第二表面112是可透光的，一外部光源(如手機螢幕所發出之光線)可以經由第二表面112輸入到血液成份分析儀100之本體102內。 When the test piece 104 collects a blood sample, the test piece 104 has a color change. The color of the test strip 104 is less susceptible to ambient light when illuminated by the screen light source of the mobile phone or by the camera attached to the mobile phone, so that the collected color is judged by the color of the test strip 104. The blood component values in the blood sample can be more accurate. To effectively block the effects of ambient light, the first surface 108 is designed to be an opaque surface and the second surface 112 is a permeable surface. Because the second surface 112 is permeable to light, an external source (such as light from a cell phone screen) can be input into the body 102 of the blood component analyzer 100 via the second surface 112.
除此之外，為了在不需要過多環境光干擾下所提供之外部光源足夠使試片104的影像得以順利地被擷取，本體102之內部表面(如第一內表面)係設置成可反射的狀態。本體102內部可另外有一光源113的設置，此光源113所發出之光線將不會經由第一表面108輸出至本體102之外，而將有機會停留在本體102內部反射，使得試片104的影像可順利地被擷取。 In addition, the internal surface of the body 102 (eg, the first inner surface) is configured to be reflective in order to provide an external source of light sufficient to allow the image of the test strip 104 to be smoothly captured without excessive ambient light interference. status. There may be another arrangement of the light source 113 inside the body 102. The light emitted by the light source 113 will not be output to the outside of the body 102 via the first surface 108, and there will be a chance to stay inside the body 102 to reflect, so that the image of the test piece 104 Can be successfully captured.
試片104上顏色之變化在不同環境溫度下彼此不同。所以本體102內部可另外設置一可隨一環境溫度變色之參考區域(未顯示)。在一個實施例中，上述參考區域係位於試片104的周邊。由於參考區域同樣因為不同環境溫度而有顏色上之改變，當試片104之影像被擷取時，參考區域的影像同樣被擷取，而能反映出因為環境溫度所造成之試片104所顯示之變化，使得不同溫度下所量測之血液範本的成份數值能夠較精確地被估算出來。 The change in color on the test piece 104 differs from one another at different ambient temperatures. Therefore, a reference area (not shown) that can change color with an ambient temperature can be additionally disposed inside the body 102. In one embodiment, the reference area described above is located at the periphery of the test strip 104. Since the reference area also has a color change due to different ambient temperatures, when the image of the test piece 104 is captured, the image of the reference area is also captured, which reflects the display of the test piece 104 due to the ambient temperature. The variation allows the component values of the blood sample measured at different temperatures to be estimated more accurately.
血液成份分析儀100可另外包含有一可撓材質層114。此可撓材質層114可以是第二表面112的一部分或是設置於第二表面112之下方，與 血液成份分析儀100所置放之物體表面(如桌面)接觸。可撓材質層114的設置，同樣可以幫助血液成份分析儀100能夠固定在所置放之物體表面，不致於產生不必要的移動，一樣可以幫助試片104對於血液範本的蒐集。 The blood component analyzer 100 can additionally include a flexible material layer 114. The flexible material layer 114 may be part of the second surface 112 or disposed below the second surface 112, and The surface of the object (such as a table top) placed on the blood component analyzer 100 is in contact. The arrangement of the flexible material layer 114 can also help the blood component analyzer 100 to be fixed on the surface of the placed object without causing unnecessary movement, which can help the sample 104 to collect blood samples.
當可撓材質層114位在第二表面112的下方時，可撓材質層114需要讓來自於外部光源的光線得以穿過(penetrable)，而穿過可撓材質層114與第二表面112的光線可以在本體102內部反射，以提供足夠的光量讓試片104與參考區域的影像可被順利擷取。 When the flexible material layer 114 is located below the second surface 112, the flexible material layer 114 needs to pass light from the external light source through the flexible material layer 114 and the second surface 112. Light can be reflected inside the body 102 to provide sufficient light to allow images of the test strip 104 and the reference area to be captured smoothly.
採血裝置106可以是以一微針陣列(micro needle array)的方式實施。可撓材質層114可以是一橡皮(rubber)或是一矽膠(silicone)組成。 The blood collection device 106 can be implemented in the form of a micro needle array. The flexible material layer 114 can be a rubber or a silicone.
請參閱第2圖，第2圖為依據本發明之一實施例的血液成份分析儀200的示意圖。血液成份分析儀200包含一本體202、一試片204位於本體202內、以及一採血裝置206同樣位於本體202內。 Please refer to FIG. 2, which is a schematic diagram of a blood component analyzer 200 in accordance with an embodiment of the present invention. The blood component analyzer 200 includes a body 202, a test strip 204 disposed within the body 202, and a blood collection device 206 located within the body 202.
本體202另外包含有一第一表面208與一第二表面212。第一表面208上之一第一預定位置係可被設計來讓採血裝置204被啟動時突出於本體202之外，以與使用者之手指有所接觸。 The body 202 further includes a first surface 208 and a second surface 212. One of the first predetermined positions on the first surface 208 can be designed to protrude beyond the body 202 when the blood collection device 204 is activated to contact the user's fingers.
第一表面208之一第二預定位置可有一開口214的設置，此開口214係透過一輸血通道216與試片204連接。當使用者之手指跟採血裝置206接觸後，血液範本能夠透過開口214與輸血通道216為試片204所蒐集。在一實施例中，輸血通道216是一毛細管，可以傳遞在開口214的血液範本至試片204。 The second predetermined position of one of the first surfaces 208 can have an opening 214 that is coupled to the test strip 204 through a blood transfusion channel 216. When the user's finger is in contact with the blood collection device 206, the blood sample can be collected for the test strip 204 through the opening 214 and the blood transfusion channel 216. In one embodiment, the blood transfusion channel 216 is a capillary that can deliver a blood sample at the opening 214 to the test strip 204.
類似於血液成份分析儀100，血液成份分析儀200之第一外表面208不可透光而其第二表面212則可以透光。如此設計，將可讓血液成份分 析儀200之本體202的內部不會有穿透第一表面208之環境光線而只有穿透第二表面212的光線在本體202的內部反射。所以，試片204(其所蒐集之血液範本同樣會因為不同溫度而有顏色之變化)與同樣設置在本體202內部之會隨著溫度變色之參考區域的影像擷取可以被順利地完成。 Similar to the blood component analyzer 100, the first outer surface 208 of the blood component analyzer 200 is non-transmissive and its second surface 212 is transparent. So designed to allow blood components to be divided The interior of the body 202 of the analyzer 200 does not have ambient light that penetrates the first surface 208 and only light that penetrates the second surface 212 is reflected within the interior of the body 202. Therefore, the test piece 204 (the blood sample collected therein will also have a color change due to different temperatures) and the image capture of the reference area which is also disposed inside the body 202 and which will change with temperature can be smoothly completed.
本體202內部可設有一內部光源218，此內部光源218所發出之光線同樣可以在本體202被設置成可反射的狀態之內部有所反射，幫助上述試片204與參考區域的影像擷取。 An internal light source 218 can be disposed inside the body 202. The light emitted by the internal light source 218 can also be reflected inside the body 202 in a reflective state to assist the image capture of the test strip 204 and the reference area.
除此之外，血液成份分析儀200可包含一可撓材質層222。此可撓材質層222可以是第二表面212的一部分或是設置在第二表面212的下方。可撓材質層222係設計成可透光之狀態，特別是當可撓材質層222設置在第二表面212的下方時。藉著提供較大之表面摩擦力，可撓材質層222亦能幫助固定整個本體202在所置放之物體表面。 In addition, blood component analyzer 200 can include a flexible material layer 222. The flexible material layer 222 can be part of the second surface 212 or disposed below the second surface 212. The flexible material layer 222 is designed to be light transmissive, particularly when the flexible material layer 222 is disposed below the second surface 212. By providing greater surface friction, the flexible material layer 222 can also help secure the entire body 202 to the surface of the object being placed.
請參閱第3圖，第3圖為依據本發明之一實施例的血液成份分析儀300的示意圖。血液成份分析儀300包含一本體302、一試片304位於本體302內、以及一採血裝置306同樣位於本體102內。 Please refer to FIG. 3, which is a schematic diagram of a blood component analyzer 300 in accordance with an embodiment of the present invention. The blood component analyzer 300 includes a body 302, a test strip 304 located within the body 302, and a blood collection device 306 located within the body 102.
本體102另外包含有一第一表面305。第一表面305上之一第一預定位置308係設計有一開口312，同時血糖試片304上之一第一預定位置314同樣有一開口316來讓採血裝置306被啟動時穿過，以與使用者之手指有所接觸。當使用者之手指跟採血裝置306接觸後得以讓血液範本能夠為血糖試片304所蒐集。試片304之第一預定位置314係對應於第一表面305的第一預定位置308，使得試片304對於血液範本的蒐集能夠順利實施。 The body 102 additionally includes a first surface 305. One of the first predetermined positions 308 on the first surface 305 is designed with an opening 312, and a first predetermined position 314 on the blood glucose test strip 304 also has an opening 316 for the blood collection device 306 to be passed through when activated. The fingers are in contact. When the user's finger is in contact with the blood collection device 306, the blood sample can be collected for the blood glucose test strip 304. The first predetermined position 314 of the test strip 304 corresponds to the first predetermined position 308 of the first surface 305 so that the collection of the test strip 304 for the blood sample can be smoothly implemented.
當試片304蒐集到血液範本時，試片304會有顏色上的變化。 而此試片304的顏色，當使用手機之螢幕光源照射或是手機之附設之照相機發出之光線照射時，較不容易受到環境光的影響，使得經由試片304的顏色而判斷所蒐集到的血液範本中之成份數值能夠較為精確。而為了有效阻絕環境光的影響，第一表面305係設計為一不透光之表面。而第二表面322則可是可透光之表面，一外部光源(如手機螢幕所發出之光線)可以經由第二表面322輸入到血液成份分析儀300之本體302內。 When the test piece 304 collects a blood sample, the test piece 304 has a color change. The color of the test strip 304 is less susceptible to ambient light when illuminated by the screen light source of the mobile phone or by the camera attached to the mobile phone, so that the collected color is judged by the color of the test strip 304. The value of the components in the blood sample can be more precise. In order to effectively block the influence of ambient light, the first surface 305 is designed as an opaque surface. The second surface 322 can be a light transmissive surface, and an external light source (such as light emitted by the mobile phone screen) can be input into the body 302 of the blood component analyzer 300 via the second surface 322.
除此之外，為了在不需要過多環境光干擾下所提供之外部光源足夠使試片304的影像得以順利地被擷取，本體302之內部表面(如第一內表面)係設置成可反射的狀態。本體302內部可另外有一光源324的設置，此光源324所發出之光線將不會經由第一表面305輸出至本體302之外，而將有機會停留在本體302內部反射，使得試片304的影像可順利地被擷取。 In addition, in order to provide an external light source provided without excessive ambient light interference sufficient for the image of the test strip 304 to be smoothly captured, the inner surface of the body 302 (such as the first inner surface) is configured to be reflective. status. There may be another light source 324 disposed inside the body 302. The light emitted by the light source 324 will not be outputted to the outside of the body 302 via the first surface 305, but will have a chance to stay inside the body 302 to reflect the image of the test piece 304. Can be successfully captured.
因為試片304上顏色之變化在不同環境溫度下彼此不同，所以本體302內部可另外設置一可隨一環境溫度變色之參考區域(未顯示)。在一個實施例中，上述參考區域係位於試片304的周邊。由於參考區域同樣因為不同環境溫度而有顏色上之改變，當試片304之影像被擷取時，參考區域的影像同樣被擷取，而能反映出因為環境溫度所造成之試片304所顯示之顏色變化，使得不同溫度下所量測之血液範本的成份數值能夠較精確地被估算出來。 Since the color variations on the test strips 304 are different from one another at different ambient temperatures, a reference area (not shown) that can be discolored with an ambient temperature can be additionally disposed within the body 302. In one embodiment, the reference area described above is located at the periphery of the test strip 304. Since the reference area also has a color change due to different ambient temperatures, when the image of the test strip 304 is captured, the image of the reference area is also captured, which reflects the display of the test strip 304 due to the ambient temperature. The color change allows the component values of the blood sample measured at different temperatures to be estimated more accurately.
血液成份分析儀300可另外包含有一可撓材質層326。此可撓材質層326可以是第二表面322的一部分或是設置於第二表面322之下方，與血液成份分析儀300所置放之物體表面(如桌面)接觸。 Blood component analyzer 300 can additionally include a layer of flexible material 326. The flexible material layer 326 can be part of the second surface 322 or disposed below the second surface 322 to contact the surface of the object (such as a table top) placed by the blood component analyzer 300.
可撓材質層326的設置，同樣可以幫助血液成份分析儀300 能夠固定在所置放之物體表面，不致於產生不必要的移動，一樣可以幫助試片304對於血液範本的蒐集。 The setting of the flexible material layer 326 can also help the blood component analyzer 300 It can be fixed on the surface of the placed object without causing unnecessary movement, which can help the test piece 304 to collect the blood sample.
當可撓材質層326位在第二表面322的下方時，可撓材質層326需要讓來自於外部光源的光線得以穿過(penetrable)，而穿過可撓材質層326與第二表面322的光線可以在本體302內部反射，以提供足夠的光量讓血糖試片304與參考區域的影像可被順利擷取。 When the flexible material layer 326 is located below the second surface 322, the flexible material layer 326 needs to pass light from the external light source through the flexible material layer 326 and the second surface 322. Light can be reflected inside the body 302 to provide sufficient light to allow the image of the blood glucose test strip 304 and the reference area to be smoothly captured.
採血裝置306如其在血糖計100與200之採血裝置106與206一樣，可以是以一微針陣列(micro needle array)的方式實施。而可撓材質層326可以是一橡皮(rubber)或是一矽膠(silicone)組成。可撓材質層326因此得以固定血液成份分析儀300在所置放的物體表面。 The blood collection device 306, like its blood collection devices 106 and 206 of the blood glucose meters 100 and 200, can be implemented in the form of a micro needle array. The flexible material layer 326 can be a rubber or a silicone. The flexible material layer 326 thus secures the blood component analyzer 300 to the surface of the object being placed.
100‧‧‧血液成份分析儀 100‧‧‧ Blood Component Analyzer
102‧‧‧本體 102‧‧‧Ontology
104‧‧‧試片 104‧‧‧ test strips
106‧‧‧採血裝置 106‧‧‧ blood collection device
108‧‧‧第一表面 108‧‧‧ first surface
112‧‧‧第二表面 112‧‧‧ second surface
113‧‧‧內部光源 113‧‧‧Internal light source
114‧‧‧可撓材質層 114‧‧‧Flexible material layer
Claims (9)
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW102128741A TWI533844B (en) | 2013-08-09 | 2013-08-09 | Blood analyte meter |
| CN201310398022.3A CN104345036B (en) | 2013-08-09 | 2013-09-04 | blood component analyzer |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW102128741A TWI533844B (en) | 2013-08-09 | 2013-08-09 | Blood analyte meter |
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| TW201505608A TW201505608A (en) | 2015-02-16 |
| TWI533844B true TWI533844B (en) | 2016-05-21 |
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| Application Number | Title | Priority Date | Filing Date |
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| TW102128741A TWI533844B (en) | 2013-08-09 | 2013-08-09 | Blood analyte meter |
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| TW (1) | TWI533844B (en) |
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| CN111551505B (en) * | 2019-07-08 | 2024-08-27 | 华中科技大学同济医学院附属协和医院 | Digital observation instrument for blood circulation of limb tissue valve |
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| US6093156A (en) * | 1996-12-06 | 2000-07-25 | Abbott Laboratories | Method and apparatus for obtaining blood for diagnostic tests |
| GB2388898B (en) * | 2002-04-02 | 2005-10-05 | Inverness Medical Ltd | Integrated sample testing meter |
| EP1929937A1 (en) * | 2006-12-07 | 2008-06-11 | F. Hoffmann-Roche AG | Device and method for investigating body fluids |
| CN201905880U (en) * | 2011-01-07 | 2011-07-27 | 郝天羽 | Household easy instrument for monitoring neonatal jaundice |
| CN201939330U (en) * | 2011-01-07 | 2011-08-24 | 郝天羽 | Network monitoring system for icterus neonatorum |
| CN201920706U (en) * | 2011-01-07 | 2011-08-10 | 郝天羽 | Home monitoring system for neonatal jaundice |
| JP2015511130A (en) * | 2012-01-10 | 2015-04-16 | サノフィ−アベンティス・ドイチュラント・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツング | Blood analysis meter |
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| TW201505608A (en) | 2015-02-16 |
| CN104345036A (en) | 2015-02-11 |
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