Incubator, Neonatal(FMZ)
新生児用インキュベーター 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。
43 件
直近 2026.06.24
86 件
0 件
867 件
分類情報
| Product Code | FMZ |
|---|---|
| デバイス名 | Incubator, Neonatal 新生児用インキュベーター 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 II |
| 21 CFR 規制番号 | 880.5400 |
| 審査区分 | 510(k)(市販前届出) |
| 医療専門分野 | 一般病院用 |
| 定義 | - |
| フラグ | 該当なし |
| AI分析 | この機器は、新生児を外部環境から保護し、体温や湿度などを一定に保つことで保育を行う医療機器です。米国ではクラスIIに分類されており、市販前届出(510(k))により既存の同等品との実質的同等性を示すことで市販が認められます。 米国市場での動向 本製品は510(k)による届出品目で、累計約90件の届出があり、参入企業は46社にのぼりますが、直近5年の届出は約5件にとどまっています。不具事報告は累計で約840件あり、内訳は不具合(Malfunction)が約660件と大半を占める一方、死亡は17件、傷害は約110件報告されており、主な問題として機器又は機器部品の脱落、流量なし、流量不足・輸液不足が挙げられています。回収は累計約40件で、うちクラスIが11件、クラスIIが約20件、クラスIIIは確認されておらず、直近5年では約20件、最新の回収は2026年5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。
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 43 件| 回収番号 | クラス | 回収開始日 | 企業 | 理由 | ステータス |
|---|---|---|---|---|---|
| Z-2477-2026 FMZ | クラス II | 2026.05.01 | GE Medical Systems, LLC | GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury. | 対応中 |
| Z-2476-2026 FMZ | クラス II | 2026.05.01 | GE Medical Systems, LLC | GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury. | 対応中 |
| Z-2475-2026 FMZ | クラス II | 2026.05.01 | GE Medical Systems, LLC | GE HealthCare has become aware of a potential issue involving the canopy soffit beneath the control panel end of the device. Under certain conditions, for example, impact during transport, one or more of the fasteners that secure the soffit can disengage. If this occurs, a fastener could fall into the patient compartment. In rare circumstances, if multiple fasteners disengage, the canopy soffit can become loose or detach. These conditions could potentially result in patient injury. | 対応中 |
| Z-0048-2025 FMZ | クラス I(最重篤) | 2024.09.03 | DATEX--OHMEDA, INC. | GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been torqued to specification. This may lead to the doors becoming loose. | 対応中 |
| Z-0047-2025 FMZ | クラス I(最重篤) | 2024.09.03 | DATEX--OHMEDA, INC. | GE HealthCare has become aware that for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices, the screw that secures the doors that cover the warmer heaters may not have been torqued to specification. This may lead to the doors becoming loose. | 対応中 |
| Z-0962-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0961-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0960-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0959-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0958-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0957-2024 FMZ | クラス I(最重篤) | 2023.12.26 | Wipro GE Healthcare Private Ltd. | GE HealthCare has become aware that the bedside panel of Care Plus, Care Plus¿ Model 1000, 2000, 3000 and 4000 Incubator, Lullaby Incubator, Lullaby TR Incubator, and Lullaby XP Incubator can be upright and look closed but not be latched if the red indicator is visible. The portholes also can look closed when not latched when the portholes are obstructed e.g., hood covers. If a patient impacts the bedside panel or porthole that is not latched, the panel can disengage and fall open, no longer protecting the patient from falling. | 対応中 |
| Z-0141-2025 FMZ | クラス I(最重篤) | 2023.06.06 | DATEX--OHMEDA, INC. | Prior to current established manufacturing practices, higher levels of airborne formaldehyde exposure from newly manufactured incubators could be seen during clinical use that would rapidly decrease over a week. Affected customers were notified in June 2023 to run incubators for a week to potentially off gas any residual airborne formaldehyde. The general scientific consensus is that sensory irritation of the eyes is the most sensitive endpoint with respect to exposure to airborne formaldehyde and is the adverse effect clinically experienced at the lowest concentration. | 完了 |
| Z-0140-2025 FMZ | クラス I(最重篤) | 2023.06.06 | DATEX--OHMEDA, INC. | Prior to current established manufacturing practices, higher levels of airborne formaldehyde exposure from newly manufactured incubators could be seen during clinical use that would rapidly decrease over a week. Affected customers were notified in June 2023 to run incubators for a week to potentially off gas any residual airborne formaldehyde. The general scientific consensus is that sensory irritation of the eyes is the most sensitive endpoint with respect to exposure to airborne formaldehyde and is the adverse effect clinically experienced at the lowest concentration. | 完了 |
| Z-2102-2023 FMZ | クラス II | 2023.05.19 | DATEX--OHMEDA, INC. | GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices | 対応中 |
| Z-2101-2023 FMZ | クラス II | 2023.05.19 | DATEX--OHMEDA, INC. | GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices | 対応中 |
| Z-2100-2023 FMZ | クラス II | 2023.05.19 | DATEX--OHMEDA, INC. | GE HealthCare has become aware of the potential that an incorrect type of secondary latch could have been installed on the northeast (NE) and/or northwest (NW) bedside panels for certain Giraffe OmniBed and Giraffe OmniBed Carestation devices | 対応中 |
| Z-2307-2021 FMZ | クラス II | 2021.06.30 | CooperSurgical, Inc. | Units are displaying output readings that differ from the measurements taken using a Gas Analyzer. When the display is reading a target setting of 5%, an external meter is reading between 3% and 12% and the Incubator does not alarm. May result in loss of embryo during storage. | 終了 |
| Z-2236-2020 FMZ | クラス II | 2020.04.28 | GE Healthcare, LLC | Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed. | 終了 |
| Z-2235-2020 FMZ | クラス II | 2020.04.28 | GE Healthcare, LLC | Potential for certain Giraffe Incubators and Giraffe OmniBeds to deliver a different environmental oxygen level than what is displayed by the device, if a certain optional component referred to as the Servo Oxygen Module is installed. | 終了 |
| Z-2111-2020 FMZ | クラス II | 2020.04.02 | GE Healthcare, LLC | During Giraffe Shuttle charging, the batteries emit low concentrations of gases (outgassing) producing a strong sulfur odor. | 終了 |
510(k)(市販前届出)
全 86 件| No. | 番号 | 機器名 | 申請者 | 決定日 | 種別 | 概要 |
|---|---|---|---|---|---|---|
| 1 | K260326 | Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1) | Datex-Ohmeda, Inc. | 2026.07.28 | 通常(Traditional) | |
| 2 | K251619 | Babyleo TN500 | Drägerwerk AG & Co. KGaA | 2026.02.13 | 通常(Traditional) | |
| 3 | K251663 | Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1) | Datex-Ohmeda, Inc. | 2025.10.22 | 通常(Traditional) | |
| 4 | K243437 | mOm Essential Incubator (ME1) | Mom Incubators Limited | 2025.08.14 | 通常(Traditional) | |
| 5 | K213553 | Giraffe Incubator Carestation CS1 | Datex Ohmeda, Inc. | 2022.03.02 | 通常(Traditional) | |
| 6 | K190494 | Infant Incubator | Ningbo David Medical Device Co., Ltd. | 2019.11.25 | 通常(Traditional) | |
| 7 | K182859 | Babyleo TN500 | Dragerwerk AG & CO Kgaa | 2019.02.22 | 特別(Special) | |
| 8 | K182977 | Isolette 8000 Plus | Draeger Medical Systems, Inc. | 2018.11.21 | 特別(Special) | |
| 9 | K172154 | Isolette 8000 plus | Draeger Medical Sytems, Inc. | 2018.04.19 | 通常(Traditional) | |
| 10 | K162821 | Babyleo TN500 | Draegerwerk AG & CO Kgaa | 2017.06.23 | 通常(Traditional) | |
| 11 | K152814 | Giraffe OmniBed Carestation CS1 | Ohmeda Medical, A Division of Datex-Ohmeda,Inc. A GE Company | 2016.03.17 | 特別(Special) | |
| 12 | K152809 | Giraffe Incubator Carestation CS1 | Ohmeda Medical, A Division of Datex-Ohmeda, Inc. | 2015.12.31 | 特別(Special) | |
| 13 | K132543 | INFANT INCUBATOR | Bistos Co., Ltd. | 2014.07.03 | 通常(Traditional) | |
| 14 | K102226 | DUAL INCU I | Atom Medical Corporation | 2011.01.04 | 通常(Traditional) | |
| 15 | K102279 | INCU I | Atom Medical Corporation | 2010.12.29 | 通常(Traditional) | |
| 16 | K102710 | NEO-SERVO I | Atom Medical Corporation | 2010.12.22 | 通常(Traditional) | |
| 17 | K101788 | GIRAFFE OMNIBED | Ohmeda Medical | 2010.07.21 | 特別(Special) | |
| 18 | K101778 | GIRAFFE INCUBATOR | Ohmeda Medical | 2010.07.21 | 特別(Special) | |
| 19 | K071977 | TARRY MEDICAL TEMPERATURE PROBES | Tarry Medical Products, Inc. | 2008.05.23 | 通常(Traditional) | |
| 20 | K072512 | MODIFICATION TO: OHMEDA MEDICAL GIRAFFE INCUBATOR (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY) | Datex-Ohmeda, Inc. | 2007.10.03 | 特別(Special) |
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)
この product code の PMA 情報はありません。
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。