Pump, Infusion, Insulin, To Be Used With Invasive Glucose Sensor(OYC)
侵襲的グルコースセンサ併用インスリン注入ポンプ この日本語名は AI が生成した参考訳です。正式名称は英語の原名です。
34 件
直近 2026.04.08
0 件
43 件
891,163 件
分類情報
| Product Code | OYC |
|---|---|
| デバイス名 | Pump, Infusion, Insulin, To Be Used With Invasive Glucose Sensor 侵襲的グルコースセンサ併用インスリン注入ポンプ この日本語名は AI が生成した参考訳です。正式名称は英語の原名です。 |
| デバイスクラス | クラス III |
| 21 CFR 規制番号 | - |
| 審査区分 | PMA(市販前承認) |
| 医療専門分野 | Unknown |
| 定義 | The insulin pump is intended to be used as a component of an invasive glucose device. The pump is designed to pump fluid (insulin) into a patient in a controlled manner as an aid in the mangement of diabetes mellitus in persons requiring insulin. It is intended to accept and display data from the glucose sensor. 本インスリンポンプは、侵襲的グルコース機器の構成要素として使用されることを意図している。本ポンプは、インスリンを必要とする者の糖尿病の管理を補助するものとして、患者に対して制御された方法で流体(インスリン)を注入するように設計されている。本ポンプは、グルコースセンサからのデータを受信し表示することを意図している。 この日本語訳は AI が生成した参考訳です。正確な内容は英語の原文をご確認ください。 |
| フラグ | 該当なし |
| AI分析 | 本品は米国においてクラスIIIに分類される医療機器であり、市販前承認(PMA)による審査を経て市場に出されます。クラスIIIは米国の医療機器分類制度の中で最も規制が厳しい区分であり、生命維持や重大な健康被害のリスクに関わる機器などが対象となり、市販前届出(510(k))よりも厳格な科学的データの提出と審査が求められます。 米国市場での動向 本品目はPMA区分の医療機器で、これまでに本承認2件、一部変更承認41件が行われており、最新の承認は2019年12月です。不具合報告は累計で約89万件と多く、その大半は不具合(Malfunction)に関するもので、死亡報告は2,249件、傷害報告は約12万7000件となっています。主な問題としてはBreak、Power Problem、Material Integrity Problemが挙げられています。回収は累計約30件で、うちクラスIが1件、クラスIIが約30件を占め、直近5年では約20件、最新の回収は2026年2月に開始されています。 この分析は公開データ(openFDA・JMDN 対応情報)をもとに AI が生成した参考情報です。市場データは2026年8月時点の集計に基づきます。 |
類似の国内医療機器(自動推定)
FDA デバイス分類と JMDN 英語名の名称・定義文の類似度から機械的に推定した候補です。日米の当局が定めた公的な対応関係ではなく、参考情報としてご覧ください。
| No. | 類別 | 一般的名称 | 品目数 | 企業数 | 年間総出荷額 | 成長率 | 平均価格 | 国産比率 |
|---|---|---|---|---|---|---|---|---|
| 1 | 医薬品注入器 | ポータブルインスリン用輸液ポンプクラスⅢ | 9 | 4 | 36.86 億円/年 | +104.7% | 7,134 円/個 | 72.3% |
| 2 | 医薬品注入器 | インスリンポンプ用輸液セットクラスⅡ | 5 | 3 | 16.29 億円/年 | +336.3% | 829 円/個 | 6.4% |
| 3 | 医薬品注入器 | 汎用輸液ポンプクラスⅢ | 49 | 13 | 30.36 億円/年 | -24.9% | 9.28 万円/個 | 92.0% |
| 4 | 内臓機能検査用器具 | インフュージョンポンプクラスⅡ | 1 | 1 | — | — | — | — |
| 5 | 医薬品注入器 | 注射筒輸液ポンプクラスⅢ | 30 | 11 | 29.72 億円/年 | -13.3% | 17.82 万円/個 | 98.8% |
FDA のデバイスクラスは 3 段階(クラス I〜III)、日本の医療機器は 4 段階(クラス I〜IV)で分類されており、 1 対 1 では対応しません。 リスク区分の考え方が異なるため、参考情報としてご利用ください。
米国での回収・承認・不具合報告
米国回収
全 34 件| 回収番号 | クラス | 回収開始日 | 企業 | 理由 | ステータス |
|---|---|---|---|---|---|
| Z-1750-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1749-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1747-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1746-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1745-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1743-2026 OYC | クラス II | 2026.02.13 | Medtronic MiniMed, Inc. | All Medtronic MiniMed infusion pumps (Paradigm series, 600 series, and BLE 700 series) were found to be affected by unintended over- and under-delivery of insulin when the pump is elevated or lowered relative to the infusion site, respectively, because of changes in gravitational force impacting hydrostatic and hydrodynamic pressures. Insulin over-delivery, which can occur when the pump is elevated relative to the infusion site, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An under-delivery of insulin, which can occur at lowered pump height conditions relative to the infusion site, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1264-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1263-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1260-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1258-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1257-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-1256-2025 OYC | クラス II | 2025.01.31 | Medtronic MiniMed, Inc. | All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and 7XX series) were found to have the potential for abnormal insulin delivery due to changes in air pressure, which can be found during airplane take-off or landing. An unexpected additional dose of insulin, which can occur during take-off, can result in severe hypoglycemia, altered mental status, seizure, coma, or death. An unexpected under-delivery of insulin, which can occur during landing, can result in severe hyperglycemia, dehydration, diabetic ketoacidosis, or death. | 対応中 |
| Z-0002-2025 OYC | クラス I(最重篤) | 2024.07.31 | Medtronic MiniMed, Inc. | Insulin pumps that have been dropped, bumped, or experienced physical impact may have damage to internal electrical components, which may cause reduced pump battery life. Since the defect reduces the battery life overall, it shortens the time between low battery alarms and increases the frequency with which the user must insert a new battery. Further, the defect may also deliver the low battery alarm when there is significantly less time before the battery completely runs out, from the expected up to 10-hour buffer the low alert is supposed to signal, leading to device powering down and stopping insulin delivery unexpectedly. Per the firm, a subset of pumps with the defect showed the low alert alarm was delivered ~2.5 hours before the device shut off, however, patient reports indicate the time could be even shorter. Replacing the battery will not resolve this issue and the short battery life and the truncated low battery alert lead time will continue to occur. Early battery depletion could result in power loss and insulin delivery could be interrupted, resulting in under delivery of insulin potentially leading to hyperglycemia and/or DKA. | 対応中 |
| Z-0194-2023 OYC | クラス II | 2022.09.20 | Medtronic MiniMed | Medtronic identified a cybersecurity vulnerability in the MiniMed 600 series Insulin Pump Systems associated with the communication protocol that could allow unauthorized access to the pump system. This unauthorized access could be used to deliver too much or too little insulin through delivery of an unintended insulin bolus or because insulin delivery is slowed or stopped, which could lead to hypoglycemia or hyperglycemia. The Remote Bolus feature on insulin pumps should be turned off to prevent the unauthorized access. | 対応中 |
| Z-1357-2022 OYC | クラス II | 2022.05.23 | Medtronic MiniMed | Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps. | 対応中 |
| Z-1356-2022 OYC | クラス II | 2022.05.23 | Medtronic MiniMed | Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps. | 対応中 |
| Z-1354-2022 OYC | クラス II | 2022.05.23 | Medtronic MiniMed | Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps. | 対応中 |
| Z-1352-2022 OYC | クラス II | 2022.05.23 | Medtronic MiniMed | Due to battery cap deterioration, this may potentially result in an incomplete battery circuit (similar to when battery cap is not attached) and a loss of power/functionality of the insulin infusion pumps. | 対応中 |
| Z-1596-2020 OYC | クラス II | 2019.06.27 | Medtronic MiniMed | The action is being initiated due to potential cybersecurity vulnerabilities related to a series of insulin pumps that are designed to communicate using a wireless radio frequency (RF). An unauthorized person could potentially connect wirelessly to a nearby insulin pump to change settings and control insulin delivery. | 対応中 |
| Z-1595-2020 OYC | クラス II | 2019.06.27 | Medtronic MiniMed | The action is being initiated due to potential cybersecurity vulnerabilities related to a series of insulin pumps that are designed to communicate using a wireless radio frequency (RF). An unauthorized person could potentially connect wirelessly to a nearby insulin pump to change settings and control insulin delivery. | 対応中 |
510(k)(市販前届出)
この product code の 510(k) 情報はありません。
出典の openFDA は各 510(k) の主要(primary)product code のみを収録しているため、副次コードを含む FDA 公式データベースの検索結果とは件数が異なる場合があります。 FDA 510(k) データベースで確認
PMA(市販前承認)
全 43 件| PMA 番号 | 販売名 | 申請者 | 決定日 |
|---|---|---|---|
| P140015/S029 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM System | Tandem Diabetes Care, Inc. | 2019.12.19 |
| P140015/S028 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM System | Tandem Diabetes Care, Inc. | 2019.03.01 |
| P140015/S027 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM | Tandem Diabetes Care, Inc. | 2018.10.26 |
| P140015/S026 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM | Tandem Diabetes Care, Inc. | 2018.10.11 |
| P130007/S036 | Animas Vibe System | Animas Corp. | 2018.07.11 |
| P140015/S025 | t:slim X2 Insulin Pump with DexcomG5 Mobile CGM System | Tandem Diabetes Care, Inc. | 2018.05.02 |
| P130007/S035 | Animas Vibe System | Animas Corp. | 2018.04.18 |
| P140015/S024 | t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM (t:slim G4 system); t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM | Tandem Diabetes Care, Inc. | 2018.04.17 |
| P130007/S034 | Animas Vibe System | Animas Corp. | 2018.03.12 |
| P130007/S033 | Animas Vibe System | Animas Corp. | 2018.03.01 |
| P140015/S023 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM | Tandem Diabetes Care, Inc. | 2018.02.14 |
| P140015/S021 | t:slim G4 Insulin Pump with Dexcom G4 Platinum CGM | Tandem Diabetes Care, Inc. | 2017.12.21 |
| P130007/S027 | Animas Vibe System | Animas Corp. | 2017.10.27 |
| P130007/S031 | Animas Vibe System | Animas Corp. | 2017.10.24 |
| P140015/S020 | t:slim X2 Insulin Pump with Dexcom G5 Mobile CGM | Tandem Diabetes Care, Inc. | 2017.08.25 |
| P130007/S029 | Animas Vibe System | Animas Corp. | 2017.08.17 |
| P140015/S022 | G4 Insulin Pump with Dexcom G4 Platinum CGM System | Tandem Diabetes Care, Inc. | 2017.06.15 |
| P130007/S026 | Animas, Vibe System | Animas Corp. | 2017.06.09 |
| P130007/S024 | Animas Vibe System | Animas Corp. | 2017.04.21 |
| P130007/S023 | Animas Vibe System | Animas Corp. | 2017.04.20 |
不具合報告(MAUDE)トレンド
米国不具合報告検索で詳しく見る出典: openFDA(U.S. FDA) のデータをそのまま掲載しています。内容の正確性・最新性は保証されません。FDA が本サイトの内容を承認・保証するものではありません。
報告の存在は、機器と事象の因果関係を意味しません。報告件数を機器間の不具合発生率の比較に用いることはできません。
各データセット(510(k)・PMA・MAUDE・回収・Warning Letter)の解説は 米国FDA情報の概要 を参照してください。
出典: openFDA(U.S. FDA) のデータをそのまま掲載しています。内容の正確性・最新性は保証されません。FDA が本サイトの内容を承認・保証するものではありません。
取得日: 2026.09.28
各データセット(510(k)・PMA・MAUDE・回収・Warning Letter)の解説は 米国FDA情報の概要 を参照してください。