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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: Zimmer Surgical, Inc. HANDPIECE, ELECTRIC DERMATOME

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Zimmer Surgical, Inc. HANDPIECE, ELECTRIC DERMATOME Back to Search Results
Catalog Number 00882100100
Medical Device Problem Code Key or Button Unresponsive/not Working (4063)
Health Effect - Clinical Code Insufficient Information (4580)
Date of Event 02/02/2026
Type of Reportable Event Malfunction
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Brand Name
HANDPIECE, ELECTRIC DERMATOME
Common Device Name
Dermatome
Manufacturer (Section D)
Zimmer Surgical, Inc.
200 west ohio avenue
dover OH 44622
Manufacturer (Section G)
Zimmer Surgical, Inc.
200 west ohio avenue
dover OH 44622
Manufacturer Contact
jennifer rapsavage
56 e. bell drive
warsaw, IN 46582
+1(574)526-0384
MDR Report Key50298989
Report Number0001526350-2026-00996
Device Sequence Number10698813
Product Code GFD
UDI-Device Identifier00889024375994
Combination Product (Y/N)N
Initial Reporter StateWI
Initial Reporter CountryUS
PMA/510(K) Number
Exempt
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Health Professional
Initial Reporter Occupation Other Health Care Professional
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
Device Catalogue Number00882100100
Device Lot Number65034001
Was Device Available for Evaluation? Yes
Date Returned to Manufacturer02/10/2026
Is the Reporter a Health Professional? Yes
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/10/2026
Initial Report FDA Received Date08/18/2026
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured03/09/2021
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 Reuse
Patient Sequence Number1
Patient SexUnknown
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