DISPOSABLE CRANIAL PERFORATOR WITH HUDSON END 14MMR SERIES Adverse Event — Report (MDR 10005)
DISPOSABLE CRANIAL PERFORATOR WITH HUDSON END 14MMR SERIES Adverse Event — Report (MDR 10005) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DISPOSABLE CRANIAL PERFORATOR WITH HUDSON END 14MMR SERIES; Manufacturer: ACRA-CUT, INC.; Report number: 10005.
| Device | DISPOSABLE CRANIAL PERFORATOR WITH HUDSON END 14MMR SERIES |
|---|---|
| Manufacturer | ACRA-CUT, INC. |
| Report number | 10005 |
| Product problem | * |
| Date received | 1994-07-21 |
| Narrative | PERFORATOR ENTERED PATIENT'S TEMPORAL LOBEINVALID DATA - REGARDING SINGLE USE LABELING OF DEVICE. PATIENT MEDICAL STATUS PRIOR TO EVENT: INVALID DATA. INVALID DATA - REGARDING MULTIPLE PATIENT INVOLVEMENT.INVALID DATA - ON DEVICE SERVICE/MAINTENANCE. NO DATA - REGARDING DATE LAST SERVICED. SERVICE PROVIDED BY: INVALID DATA. INVALID DATA - SERVICE RECORDS AVAILABILITY.INVALID DATA - REGARDING WHETH |
| Source | openFDA MAUDE (device adverse events) |
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