• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: B. Braun Medical Inc. Infusomat®; SET, ADMINISTRATION, INTRAVASCULAR

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

B. Braun Medical Inc. Infusomat®; SET, ADMINISTRATION, INTRAVASCULAR Back to Search Results
Catalog Number 490100
Medical Device Problem Code Leak/Splash (1354)
Health Effect - Clinical Code Chemical Exposure (2570)
Type of Reportable Event Malfunction
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
Infusomat®
Common Device Name
SET, ADMINISTRATION, INTRAVASCULAR
Manufacturer (Section D)
B. Braun Medical Inc.
824 12th ave
bethlehem PA 18018
Manufacturer (Section G)
B. Braun Medical Inc.
824 12th ave
bethlehem PA 18018
Manufacturer Contact
elena reifenstein
824 12th ave
bethlehem, PA 18018
+1(833)425-1464
MDR Report Key50429375
Report Number2521402-2026-00812
Device Sequence Number18436291
Product Code FPA
UDI-Device Identifier04046964186080
UDI-Public(01)04046964186080
Combination Product (Y/N)N
Initial Reporter StateCA
Initial Reporter CountryUS
PMA/510(K) Number
K142036
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional,User Facility
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial,Followup
Report Date (Section B) 09/18/2026
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 Catalogue Number490100
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/17/2026
Supplement Date Received by ManufacturerNot provided
Initial Report FDA Received Date08/25/2026
Supplement Report FDA Received Date09/18/2026
Was Device Evaluated by Manufacturer? (Y/N) No
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 Number1
Patient SexUnknown
-
-