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。

米国回収

43 件

直近 2026.06.24

510(k)

86 件

PMA

0 件

不具合報告

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。

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保育器開放式保育器クラスⅡ11————
2保育器定置型保育器クラスⅢ20611.73 億円/年-18.7% 108.33 万円/個97.7%
3医療用定温器哺乳瓶保温器クラスⅠ11————
4内臓機能検査用器具新生児モニタクラスⅡ——————
5保育器運搬用保育器クラスⅢ422.93 億円/年-30.5% 75.86 万円/個99.3%

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

無料会員 1,000名 突破

回収・承認・不具合報告の明細の閲覧は会員限定です

無料で会員登録する
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 II2026.05.01GE 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 II2026.05.01GE 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 II2026.05.01GE 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)2024.09.03DATEX--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)2024.09.03DATEX--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)2023.12.26Wipro 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)2023.12.26Wipro 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)2023.12.26Wipro 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)2023.12.26Wipro 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)2023.12.26Wipro 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)2023.12.26Wipro 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)2023.06.06DATEX--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)2023.06.06DATEX--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 II2023.05.19DATEX--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 II2023.05.19DATEX--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 II2023.05.19DATEX--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 II2021.06.30CooperSurgical, 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 II2020.04.28GE 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 II2020.04.28GE 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 II2020.04.02GE 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
1K260326 Giraffe™ OmniBed™ Carestation (CS1); Giraffe™ Incubator Carestation (CS1)Datex-Ohmeda, Inc.2026.07.28通常(Traditional) PDF
2K251619 Babyleo TN500Drägerwerk AG & Co. KGaA2026.02.13通常(Traditional) PDF
3K251663 Giraffe OmniBed Carestation (CS1); Giraffe Incubator Carestation (CS1)Datex-Ohmeda, Inc.2025.10.22通常(Traditional) PDF
4K243437 mOm Essential Incubator (ME1)Mom Incubators Limited2025.08.14通常(Traditional) PDF
5K213553 Giraffe Incubator Carestation CS1Datex Ohmeda, Inc.2022.03.02通常(Traditional) PDF
6K190494 Infant IncubatorNingbo David Medical Device Co., Ltd.2019.11.25通常(Traditional) PDF
7K182859 Babyleo TN500Dragerwerk AG & CO Kgaa2019.02.22特別(Special) PDF
8K182977 Isolette 8000 PlusDraeger Medical Systems, Inc.2018.11.21特別(Special) PDF
9K172154 Isolette 8000 plusDraeger Medical Sytems, Inc.2018.04.19通常(Traditional) PDF
10K162821 Babyleo TN500Draegerwerk AG & CO Kgaa2017.06.23通常(Traditional) PDF
11K152814 Giraffe OmniBed Carestation CS1Ohmeda Medical, A Division of Datex-Ohmeda,Inc. A GE Company2016.03.17特別(Special) PDF
12K152809 Giraffe Incubator Carestation CS1Ohmeda Medical, A Division of Datex-Ohmeda, Inc.2015.12.31特別(Special) PDF
13K132543 INFANT INCUBATORBistos Co., Ltd.2014.07.03通常(Traditional) PDF
14K102226 DUAL INCU IAtom Medical Corporation2011.01.04通常(Traditional) PDF
15K102279 INCU IAtom Medical Corporation2010.12.29通常(Traditional) PDF
16K102710 NEO-SERVO IAtom Medical Corporation2010.12.22通常(Traditional) PDF
17K101788 GIRAFFE OMNIBEDOhmeda Medical2010.07.21特別(Special) PDF
18K101778 GIRAFFE INCUBATOROhmeda Medical2010.07.21特別(Special) PDF
19K071977 TARRY MEDICAL TEMPERATURE PROBESTarry Medical Products, Inc.2008.05.23通常(Traditional) PDF
20K072512 MODIFICATION TO: OHMEDA MEDICAL GIRAFFE INCUBATOR (GIRAFFE AND PANDA UNINTERRUPTIBLE POWER SUPPLY)Datex-Ohmeda, Inc.2007.10.03特別(Special) PDF

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。

不具合報告データを読み込み中...

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。