MAUDE Adverse Event Report: Knittel Glaser SLIDE BOND APEX ADHESIVE; Slides, Microscope

Model Number	SLIDE BOND APEX ADHESIVE
Medical Device Problem Codes	Adverse Event Without Identified Device or Use Problem (2993); Insufficient Device Problem Information (3190)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	06/30/2026
Type of Reportable Event	Malfunction

• Brand Name: SLIDE BOND APEX ADHESIVE
• Common Device Name: Slides, Microscope
• Manufacturer (Section D): Knittel Glaser; varrentrappstraße 3-5; braunschweig 00000 3811; GM 0000038114
• Manufacturer (Section G): Knittel Glaser; varrentrappstraße 3-5; braunschweig 00000 3811; GM 0000038114
• Manufacturer Contact: heather jensen ; 5205 us-12; richmond, IL 60071 ; +1(815)298-8371
• MDR Report Key: 50094506
• Report Number: 1419341-2026-00009
• Device Sequence Number: 21452322
• Product Code: KEW
• UDI-Device Identifier: 20849832016438
• UDI-Public: 20849832016438
• Combination Product (Y/N): N
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 08/11/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Expiration Date: 07/20/2026
• Device Model Number: SLIDE BOND APEX ADHESIVE
• Device Catalogue Number: 3800040
• Device Lot Number: 4900080253
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 06/30/2026
• Supplement Date Received by Manufacturer: 08/06/2026
• Initial Report FDA Received Date: 07/31/2026
• Supplement Report FDA Received Date: 08/12/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 04/24/2026
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown