Brand Name | ZIMMER AIR DERMATOME |
Type of Device | 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
|
5745260384
|
|
MDR Report Key | 18761778 |
MDR Text Key | 336024127 |
Report Number | 0001526350-2024-00263 |
Device Sequence Number | 1 |
Product Code |
GFD
|
Combination Product (y/n) | N |
Reporter Country Code | MX |
PMA/PMN Number | EXEMPT |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
02/22/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/22/2024 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | N/A |
Device Catalogue Number | 00880100100 |
Device Lot Number | N/A |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 01/29/2024 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Removal/Correction Number | N/A |
Patient Sequence Number | 1 |
Treatment | DERMATOME BLADEPN: 00880000010LN: 65201360; UNK PNEUMATIC HOSEPN: UNKLN: 65536881 |
Patient Sex | Prefer Not To Disclose |