MAUDE Adverse Event Report: Maquet GmbH MEERA mobile operating table; Table, Operating-Room, Ac-Powered

Model Number	720001B0
Medical Device Problem Code	Use of Device Problem (1670)
Health Effect - Clinical Code	Crushing Injury (1797)
Date of Event	08/19/2026
Type of Reportable Event	Serious Injury

• Brand Name: MEERA mobile operating table
• Common Device Name: Table, Operating-Room, Ac-Powered
• Manufacturer (Section D): Maquet GmbH; kehler strasse 31; rastatt ; GM
• Manufacturer (Section G): Maquet GmbH; kehler strasse 31; rastatt ; GM
• Manufacturer Contact: diana gutekunst ; kehler strasse 31; rastatt ; GM
• MDR Report Key: 50777168
• Report Number: 3013876692-2026-00103
• Device Sequence Number: 10708075
• Product Code: FQO
• UDI-Device Identifier: 04046768124332
• UDI-Public: (01)04046768124332
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Importer
• Report Source: Foreign,User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 09/15/2026
• Report Date (Section F): 09/15/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 720001B0
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Distributor Facility Aware Date: 08/20/2026
• Device Age: 8 YR
• Date Report to Manufacturer: 09/15/2026
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: Not provided
• Initial Report FDA Received Date: 09/15/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/18/2018
• Is the Device Labeled for Single Use? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown
• Date Report Sent to FDA: 09/15/2026