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JPH056466B2 - - Google Patents

Info

Publication number
JPH056466B2
JPH056466B2 JP62266145A JP26614587A JPH056466B2 JP H056466 B2 JPH056466 B2 JP H056466B2 JP 62266145 A JP62266145 A JP 62266145A JP 26614587 A JP26614587 A JP 26614587A JP H056466 B2 JPH056466 B2 JP H056466B2
Authority
JP
Japan
Prior art keywords
concentrate
pump
dialysate
conductivity
stroke
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
JP62266145A
Other languages
Japanese (ja)
Other versions
JPS63164959A (en
Inventor
Robaato Shoorudeisu Deebitsudo
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Terumo BCT Inc
Original Assignee
Cobe Laboratories Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cobe Laboratories Inc filed Critical Cobe Laboratories Inc
Publication of JPS63164959A publication Critical patent/JPS63164959A/en
Publication of JPH056466B2 publication Critical patent/JPH056466B2/ja
Granted legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A61M1/1654Dialysates therefor
    • A61M1/1656Apparatus for preparing dialysates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M1/00Suction or pumping devices for medical purposes; Devices for carrying-off, for treatment of, or for carrying-over, body-liquids; Drainage systems
    • A61M1/14Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis
    • A61M1/16Dialysis systems; Artificial kidneys; Blood oxygenators ; Reciprocating systems for treatment of body fluids, e.g. single needle systems for hemofiltration or pheresis with membranes
    • A61M1/1654Dialysates therefor
    • A61M1/1656Apparatus for preparing dialysates
    • A61M1/166Heating
    • A61M1/1662Heating with heat exchange between fresh and used dialysate

Landscapes

  • Health & Medical Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Vascular Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Emergency Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • External Artificial Organs (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、透析濃縮液と水とを混合する透析液
製造装置に係る。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a dialysis fluid production device that mixes dialysis concentrate and water.

(従来の技術) ジヨンソン氏の米国特許第4371185号(本明細
書中にて引用例として参照されている)に示した
型式の透析液製造装置では、水は加熱され、空気
を分離され、そして透析濃縮液と混合され、患者
の使用している透析器に透析液を連続して供給す
るようになつている。そうした装置では、透析液
は一般に主要送り配管の途中にある合流部にポン
プ輸送され水と混合される。下流側には伝導率検
知セルが用いられ、この伝導率検知セルを通り抜
ける混合溶液の伝導率を検知し(伝導率は水に含
まれる透析成分の濃度に関係している)、この検
知した伝導率を制御ループに用いた透析濃縮液用
のポンプを制御している。この装置を滅菌したり
洗浄して別の患者に使用する際、透析液製造装置
の水圧回路は消毒剤や殺菌剤で洗い流される。
BACKGROUND OF THE INVENTION In a dialysate production apparatus of the type shown in Johnsson U.S. Pat. No. 4,371,185 (which is incorporated herein by reference), water is heated, air is separated, and It is mixed with dialysis concentrate to provide a continuous supply of dialysate to the patient's dialyzer. In such devices, dialysate is typically pumped to a junction in the main delivery line and mixed with water. A conductivity detection cell is used on the downstream side to detect the conductivity of the mixed solution passing through the conductivity detection cell (conductivity is related to the concentration of dialysate components in the water). The pump for dialysis concentrate is controlled using the rate in the control loop. When the device is sterilized or cleaned for use on another patient, the hydraulic circuit of the dialysate production device is flushed with a disinfectant or disinfectant.

(問題点を解決するための手段) 透析液製造装置は、容積式ポンプを用いること
によりさらに安全性を高められる(例えば、有害
な化学物質が添加されるのを防止できる)ことが
判明した。前記容積式ポンプはストローク当たり
の吐出し量が一定していて、水の流れている主要
送り配管に濃縮液をポンプ輸送することができ
る。容積式ポンプは、主要送り配管の下流側にあ
る濃度センサーとコントローラを用いフイードバ
ツクループによつて制御されている。前記コント
ローラは、ポンプのストローク比を予め定められ
た作動ストローク比の範囲と比較するようになつ
ている。
(Means for Solving the Problems) It has been found that the safety of the dialysate production apparatus can be further improved (for example, the addition of harmful chemicals can be prevented) by using a positive displacement pump. The positive displacement pump has a constant displacement per stroke and is capable of pumping concentrate into a main feed line carrying water. Positive displacement pumps are controlled by a feedback loop using a concentration sensor and controller downstream of the main feed line. The controller is adapted to compare the stroke ratio of the pump to a predetermined range of operating stroke ratios.

好ましい実施例では、濃度センサーには伝導率
センサーが使われる。また濃縮液ポンプは、濃縮
液の供給源または洗浄化学薬品の供給源のいずれ
か一方に連結することができる。濃縮液に対する
予め定められたの作動ストローク比の範囲は、伝
導率設定値を得るのに要する洗浄化学薬品のポン
プ比を含んでいない。
In a preferred embodiment, the concentration sensor is a conductivity sensor. The concentrate pump can also be connected to either a source of concentrate or a source of cleaning chemicals. The predetermined operating stroke ratio range for the concentrate does not include the cleaning chemical pump ratio required to achieve the conductivity set point.

本発明の他の利点並びに特徴は、本発明の以下
の好ましい実施例の説明並びに特許請求の範囲か
ら明らかになる。
Other advantages and features of the invention will become apparent from the following description of preferred embodiments of the invention, as well as from the claims.

好ましい実施例を説明する。 A preferred embodiment will now be described.

(実施例) 構 造 図面を参照する。図示の透析液製造装置10
は、給水源に連絡する端部14と患者の血液を透
析するための透析器18の流入口16に連結され
る別の端部とを持つ主要送り配管12を備えてい
る。透析器18は、患者に連結される血液の流入
口20および血液の流出口22と透析液の流出口
24とを備えている。濃縮液送り配管26は一端
が主要送り配管12の合流部28に連結され、ま
た他端には透析濃縮液(アセタート)容器36ま
たは洗浄流体(消毒剤)容器38と択一的に連絡
できるよう、容器36の取付部32との接続で解
除して容器38の取付部34に接続可能なコネク
タ30を備えている。
(Example) Structure Please refer to the drawings. Illustrated dialysate manufacturing apparatus 10
comprises a main feed line 12 having an end 14 communicating with a water supply and another end connected to an inlet 16 of a dialyzer 18 for dialyzing the patient's blood. The dialyzer 18 includes a blood inlet 20 and a blood outlet 22 connected to the patient, and a dialysate outlet 24. The concentrate feed line 26 is connected at one end to a confluence 28 of the main feed line 12 and at the other end for communication with either a dialysis concentrate (acetate) container 36 or a cleaning fluid (disinfectant) container 38 . , a connector 30 that can be disconnected from the attachment part 32 of the container 36 and connected to the attachment part 34 of the container 38 is provided.

濃縮液送り配管26には、ストローク当たり一
定の吐出し量の容積式ダイアフラムポンプ40が
設けられている。主要送り配管12の合流部28
から下流側には混合室42と伝導率検知セル44
が設けられている。ポンプ40は、センサー44
で検知された伝導率に基づいてフイードバツクル
ープによつて制御される。このフイードバツクル
ープは、図中ではコントローラ48に延びる点線
で示す配線46およびポンプ40に延びる点線で
示す配線47により表わされている。コントロー
ラ48は比較器を備え、この比較器によりポンプ
40のストローク比(ストローク/時間)(すな
わち、配線47を通じてポンプ40に送られるパ
ルスの割合)と、予め定められた作動ストローク
比の範囲を表わす限界値とを比較するようになつ
ている。
The concentrate feed pipe 26 is provided with a positive displacement diaphragm pump 40 that has a constant discharge amount per stroke. Merging section 28 of main feed pipe 12
On the downstream side there is a mixing chamber 42 and a conductivity detection cell 44.
is provided. The pump 40 has a sensor 44
controlled by a feedback loop based on the sensed conductivity. This feedback loop is represented in the figure by a dotted line 46 extending to the controller 48 and a dotted line 47 extending to the pump 40. The controller 48 includes a comparator that represents the stroke ratio (strokes/time) of the pump 40 (i.e., the rate of pulses sent to the pump 40 via line 47) and a predetermined range of operating stroke ratios. It is designed to compare with the limit value.

また装置10は、熱交換器、加熱器組込み空気
分離器、(透析器に流入する流れと透析器から流
出する流れとを平衡させ、限界濾過を管理する)
平衡室、別の伝導率検知セルおよびPHセンサーを
備えている。これらはすべて図示されていない。
さらにこの装置は、第2の濃縮液送り配管(ポン
プおよび容器コネクタを装備している)と合流
部、そして混合室と伝導率検知セルを備えてい
る。これらすべては合流部28から上流側にあ
り、この別系統の送り配管を用いて重炭酸塩を添
加し、また配管26を通じて酸を加え、アセター
トの代わりに重炭酸塩と酸の溶液を使用すること
ができる。
The device 10 also includes a heat exchanger, an air separator with a heater (which balances the flow into and out of the dialyzer, and manages ultrafiltration).
It is equipped with an equilibrium chamber, a separate conductivity sensing cell and a PH sensor. All these are not shown.
The device further includes a second concentrate delivery line (equipped with a pump and vessel connector) and a junction, as well as a mixing chamber and a conductivity sensing cell. All of this is upstream from the confluence 28, and this separate feed line is used to add bicarbonate and the acid is added through line 26, using a solution of bicarbonate and acid instead of acetate. be able to.

操 作 操作に際し、水が端部14から送り配管12に
流され、また透析濃縮液がポンプ40により合流
部28にポンプ輸送される。この合流部28の位
置で水は濃縮液と初期混合される。混合室42内
でさらに攪拌が行われる。混合室42は真空ポン
プ(図示せず)に連結された排気孔を備え、溶液
から抜け出たガスを除去するようになつている。
混合された透析濃縮液/水溶液は混合室42から
伝導率検知セル44を通り抜け、この伝導率検知
セルから透析器18の透析膜の透析側へと流れて
行く。センサー44で検知された伝導率はフイー
ドバツクされ、そしてポンプ40を制御するのに
用いられ、予め定められた透析濃度に見合う伝導
率を得ている。ポンプ40のストローク比はコン
トローラ48により自動的にモニターされ、この
コントローラ48がモニターしたストローク比を
特定の濃度における予め定められた作動ストロー
クの範囲と連続的に比較するようになつている。
Operation In operation, water is flowed from end 14 into feed line 12 and dialysis concentrate is pumped to junction 28 by pump 40. At this junction 28, the water is initially mixed with the concentrate. Further stirring is performed within the mixing chamber 42. The mixing chamber 42 is equipped with an exhaust port connected to a vacuum pump (not shown) to remove gases escaping from the solution.
The mixed dialysis concentrate/aqueous solution flows from the mixing chamber 42 through the conductivity sensing cell 44 and from the conductivity sensing cell to the dialysis side of the dialysis membrane of the dialyzer 18. The conductivity sensed by sensor 44 is fed back and used to control pump 40 to obtain a conductivity that matches a predetermined dialysis concentration. The stroke ratio of pump 40 is automatically monitored by controller 48, which continuously compares the monitored stroke ratio to a predetermined operating stroke range at a particular concentration.

異なつた患者に転用する際、水圧回路は水で水
洗され、そして洗浄流体で洗い流される。洗浄流
体の一部はある期間にわたり回路内に残留するこ
とがある。本明細書中で使用した「洗浄流体」と
は、装置系を通じて洗い流すことのできる消毒剤
や殺菌剤またはその他の化学薬品を意味してい
る。例えば図面に示すように、容器38の取付部
34にコネクタ30を連結した後に、容器38の
消毒剤によりポンプ40を用いている装置系を洗
浄する。
When transferred to a different patient, the hydraulic circuit is flushed with water and flushed with cleaning fluid. Some of the cleaning fluid may remain in the circuit for a period of time. As used herein, "cleaning fluid" refers to a disinfectant, disinfectant, or other chemical that can be flushed through a device system. For example, as shown in the drawings, after connecting the connector 30 to the attachment portion 34 of the container 38, the system using the pump 40 is cleaned with the disinfectant in the container 38.

コントローラ48によりストローク容積を連続
的にモニターすることで、伝導率設定値に適合す
ることがありしかも患者にとつて有害な不適当な
化学薬品が誤つて使用されるのを防ぐことができ
る。例えば透析濃縮液をポンプ輸送し、この透析
濃縮液と水とを1:34になるように混合し、混合
してでき上がつた溶液の伝導率を設定値として使
用する。ポンプのストローク比が1:20のポンプ
動作をするようになれば、限界値を越えたものと
してコントローラ48から警報手段(図示せず)
に出力が与えられ、警報が鳴らされる。消毒剤を
ポンプ輸送して伝導率を設定値に近づけるには、
1:20の混合割合に付随したストローク比よりも
高いストローク比でポンプ輸送する必要がある。
Continuous monitoring of stroke volume by controller 48 prevents the inadvertent use of inappropriate chemicals that may meet conductivity settings and be harmful to the patient. For example, a dialysis concentrate is pumped, the dialysis concentrate and water are mixed at a ratio of 1:34, and the conductivity of the resulting solution is used as a set value. When the pump operates at a stroke ratio of 1:20, the controller 48 issues an alarm (not shown) as the limit value has been exceeded.
is given an output and an alarm is sounded. To pump the disinfectant and bring the conductivity closer to the set point,
It is necessary to pump at a higher stroke ratio than that associated with a 1:20 mix ratio.

ループ46が容器36内の濃縮液濃度の変化を
自動的に補正する他の利点も得られる。
Another advantage is that loop 46 automatically compensates for changes in concentrate concentration within container 36.

本発明のその他の実施例は特許請求の範囲に含
まれている。
Other embodiments of the invention are within the scope of the claims.

【図面の簡単な説明】[Brief explanation of drawings]

図面は、本発明に係る透析液製造装置の概略説
明図である。 10……透析液製造装置、12……主要送り配
管、14……配管の端部、16……透析器の流入
口、18……透析器、20……透析器の血液の流
入口、22……透析器の血液の流出口、24……
透析液の流出口、26……濃縮液送り配管、28
……合流部、30……コネクタ、32,34……
取付部、36……透析濃縮液容器、38……消毒
剤容器、40……ポンプ、42……混合室、44
……伝導率検知セル、46,47……配線、48
……コントローラ。
The drawing is a schematic explanatory diagram of a dialysate manufacturing apparatus according to the present invention. DESCRIPTION OF SYMBOLS 10... Dialysate manufacturing device, 12... Main feed piping, 14... Piping end, 16... Dialyzer inlet, 18... Dialyzer, 20... Blood inlet of dialyzer, 22 ...Blood outlet of the dialyzer, 24...
Dialysate outlet, 26...Concentrate feed piping, 28
... Merging section, 30 ... Connector, 32, 34 ...
Attachment part, 36... Dialysis concentrate container, 38... Disinfectant container, 40... Pump, 42... Mixing chamber, 44
...Conductivity detection cell, 46, 47...Wiring, 48
……controller.

Claims (1)

【特許請求の範囲】 1 透析濃縮液と水とを混合する透析液製造装置
にして、当該装置は、 給水源に連絡する一方の端部、および患者の血
液を透析するための透析器に透析液を供給する別
の端部を備えている主要送り配管と、 透析濃縮液の供給源に連絡する一方の端部、お
よび前記主要送り配管の合流部に連絡されていて
当該主要送り配管内の水に濃縮液を加えることの
できる別の端部を備えている濃縮液送り配管と、 当該濃縮液送り配管の途中にあつてストローク
当たりの吐出し量が一定した容積式ポンプと、 前記合流部から下流則の前記主要送り配管の途
中にあつて、濃縮液をポンプ輸送させるための制
御信号を前記ポンプに送り予め定められた濃度を
得るための濃度センサーと、 前記ポンプのストローク比と予め定められた作
動ストローク比の範囲を表わす限界値とを比較す
る比較器を備え、前記ポンプのストローク比が前
記限界値を越えたときに警報手段に出力を与える
ようになされているコントローラとを有している
透析液製造装置。 2 特許請求の範囲第1項に記載の透析液製造装
置において、前記濃度センサーはある伝導率設定
値を持つ伝導率センサーであり、この伝導率設定
値が前記予め定められたの濃度に対応する値に関
連づけられている透析液製造装置。 3 特許請求の範囲第2項に記載の透析液製造装
置において、前記濃縮液送り配管の前記一方の端
部は、前記透析濃縮液の供給源との接続を解除し
て洗浄流体の供給源に接続可能なコネクタを備
え、また前記濃縮液に対する予め定められた作動
ストローク比の範囲を表わす限界値は、前記洗浄
流体をポンプ輸送して前記伝導率設定値の得られ
る比率を含んでいない透析液製造装置。
[Scope of Claims] 1. A dialysate manufacturing device for mixing dialysis concentrate and water, the device having: one end communicating with a water supply source and a dialyzer for dialyzing the blood of a patient; a main feed line having another end for supplying fluid; one end communicating with a source of dialysis concentrate; A concentrate feed pipe having another end capable of adding concentrate to water; a positive displacement pump located in the middle of the concentrate feed pipe and having a constant discharge amount per stroke; and the merging section. A concentration sensor located in the middle of the main feed pipe downstream from the pump, for sending a control signal to the pump to obtain a predetermined concentration for pumping the concentrated liquid; and a controller for comparing the stroke ratio of the pump with a limit value representing a range of operating stroke ratios, the controller being configured to provide an output to alarm means when the stroke ratio of the pump exceeds the limit value. Dialysate manufacturing equipment. 2. In the dialysate manufacturing apparatus according to claim 1, the concentration sensor is a conductivity sensor having a certain conductivity setting value, and this conductivity setting value corresponds to the predetermined concentration. The dialysate production equipment associated with the value. 3. In the dialysate manufacturing apparatus according to claim 2, the one end of the concentrate feed pipe is disconnected from the dialysis concentrate supply source and connected to the cleaning fluid supply source. A dialysate having a connectable connector and a limit value representing a range of predetermined operating stroke ratios for said concentrate that does not include the resulting ratio of said conductivity set point by pumping said wash fluid. Manufacturing equipment.
JP62266145A 1986-10-30 1987-10-21 Dialytic liquid preparing apparatus Granted JPS63164959A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US92588586A 1986-10-30 1986-10-30
US925885 1986-10-30

Publications (2)

Publication Number Publication Date
JPS63164959A JPS63164959A (en) 1988-07-08
JPH056466B2 true JPH056466B2 (en) 1993-01-26

Family

ID=25452390

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62266145A Granted JPS63164959A (en) 1986-10-30 1987-10-21 Dialytic liquid preparing apparatus

Country Status (5)

Country Link
JP (1) JPS63164959A (en)
CA (1) CA1293127C (en)
DE (1) DE3736711A1 (en)
FR (1) FR2605894B1 (en)
GB (1) GB2201354B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2242181B (en) * 1990-03-20 1994-02-02 Whitbread & Co Plc A fluid dosing and mixing system

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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Also Published As

Publication number Publication date
FR2605894A1 (en) 1988-05-06
CA1293127C (en) 1991-12-17
GB2201354A (en) 1988-09-01
FR2605894B1 (en) 1991-09-13
GB8725435D0 (en) 1987-12-02
DE3736711A1 (en) 1988-05-19
JPS63164959A (en) 1988-07-08
GB2201354B (en) 1990-05-02
DE3736711C2 (en) 1991-11-21

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