| Brand Name | ZIMMER AIR 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 Key | 50283152 |
| Report Number | 0001526350-2026-00988 |
| Device Sequence Number | 10442543 |
| Product Code |
GFD
|
| UDI-Device Identifier | 00889024375901 |
| UDI-Public | (01)00889024375901(11)190823(10)64479178 |
| Combination Product (Y/N) | N |
| Initial Reporter State | OH |
| Initial Reporter Country | US |
| PMA/510(K) Number | Exempt |
| Number of Events Summarized | 1 |
| 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) |
08/17/2026 |
| 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 Number | 00880100100 |
| Device Lot Number | 64479178 |
| Was Device Available for Evaluation? |
Yes
|
| Date Returned to Manufacturer | 03/16/2026 |
| 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 | 08/17/2026 |
| Initial Report FDA Received Date | 08/17/2026 |
| Was Device Evaluated by Manufacturer? (Y/N) |
Yes
|
| Date Device Manufactured | 08/23/2019 |
| 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 Number | 1 |
| Patient Sex | Unknown |
|
|