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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: BOSTON SCIENTIFIC CORPORATION Gladiator? Elite; Catheter, Angioplasty, Peripheral, Transluminal

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BOSTON SCIENTIFIC CORPORATION Gladiator? Elite; Catheter, Angioplasty, Peripheral, Transluminal Back to Search Results
Model Number H74939207030440
Medical Device Problem Code Material Rupture (1546)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 07/24/2026
Type of Reportable Event Malfunction
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Brand Name
Gladiator? Elite
Common Device Name
Catheter, Angioplasty, Peripheral, Transluminal
Manufacturer (Section D)
BOSTON SCIENTIFIC CORPORATION
300 boston scientific way
marlborough MA 01752
Manufacturer (Section G)
Boston Scientific Corporation
pmt 741 persiaran cassia selat
bandarcassia, pulau pinan 14110
MY   14110
Manufacturer Contact
mark mischke
4100 hamline ave n
arden hills, MN 55112
+1(763)494-1632
MDR Report Key50295719
Report Number2124215-2026-44302
Device Sequence Number10733154
Product Code LIT
UDI-Device Identifier08714729809562
Combination Product (Y/N)N
Initial Reporter CountryCH
PMA/510(K) Number
K132810
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Other,Foreign,Health Professional,Company Representative,Distributor
Initial Reporter Occupation Physician
Type of Report Initial
Report Date (Section B) 08/18/2026
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 Model NumberH74939207030440
Device Catalogue NumberH74939207030440
Device Lot Number0037327787
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 07/25/2026
Initial Report FDA Received Date08/18/2026
Date Device Manufactured08/29/2025
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 Age40 YR
Patient SexMale
Patient Weight143 LB
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