MAUDE Adverse Event Report: HANDSWITCH; UNIT, OPERATIVE DENTAL

Model Number 5100009000

Device Problem Device Remains Activated (1525)

Patient Problems No Patient Involvement (2645); No Clinical Signs, Symptoms or Conditions (4582)

Event Date 06/30/2020

Event Type  malfunction  

Manufacturer Narrative

This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events: 1 event was reported for this quarter.Product return status: 1 device investigation type has not yet been determined.Additional information: 1 device was not labeled for single-use.1 device was not reprocessed or reused.

Event Description

This report summarizes 1 malfunction event in which the device had run-on.1 event had no patient involvement; no patient impact.

Manufacturer Narrative

This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.1 previously reported event is included in this follow-up record.Product return status: 1 device was not available for evaluation.H3 other text : device not available.

Event Description

This report summarizes 1 malfunction event in which the device had run-on.1 event had no patient involvement; no patient impact.

• Brand Name: HANDSWITCH
• Type of Device: UNIT, OPERATIVE DENTAL
• MDR Report Key: 10329666
• MDR Text Key: 200786763
• Report Number: 0001811755-2020-01835
• Device Sequence Number: 1
• Product Code: EIA
• UDI-Device Identifier: 04546540074393
• UDI-Public: 04546540074393
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): Y
• Report Source: Manufacturer
• Source Type: company representative
• Type of Report: Initial,Followup
• Report Date: 07/29/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 07/27/2020
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: No Information
• Device Model Number: 5100009000
• Device Catalogue Number: 5100009000
• Device Lot Number: VMSR
• Was Device Available for Evaluation?: No
• Date Manufacturer Received: 06/30/2020
• Was Device Evaluated by Manufacturer?: No
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1