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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: KARL STORZ SE & Co. KG Uretero-Renoscope, 7 Fr., 6°, 43 cm

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KARL STORZ SE & Co. KG Uretero-Renoscope, 7 Fr., 6°, 43 cm Back to Search Results
Model Number 27000L
Medical Device Problem Code Poor Quality Image (1408)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event Malfunction
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Brand Name
Uretero-Renoscope, 7 Fr., 6°, 43 cm
Common Device Name
Uretero-Renoscope, 7 Fr., 6°, 43 cm
Manufacturer (Section D)
KARL STORZ SE & Co. KG
dr.-karl-storz-strasse 34
tuttlingen 78532
Manufacturer (Section G)
KARL STORZ SE & Co. KG
dr.-karl-storz-strasse 34
tuttlingen, 78532
GM   78532
Manufacturer Contact
theresa mussaw
2151 e grand ave
el segundo, CA 90245
+1(410)441-1327
MDR Report Key50354441
Report Number9610617-2026-02005
Device Sequence Number13309392
Product Code FGB
UDI-Device Identifier04048551311271
UDI-Public04048551311271
Combination Product (Y/N)N
Initial Reporter CountryIT
PMA/510(K) Number
K233372
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,Health Professional,Company Representative
Initial Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date (Section B) 08/20/2026
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 Number27000L
Device Catalogue Number27000L
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer07/27/2026
Is the Reporter a Health Professional? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer Not provided
Initial Report FDA Received Date08/20/2026
Was Device Evaluated by Manufacturer? (Y/N) No
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device Unknown
Patient Sequence Number1
Patient SexUnknown
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