MICRUSFRAME10 6MM X 26CM Adverse Event — Malfunction (MDR 3008114965-2020-00145)
MICRUSFRAME10 6MM X 26CM Adverse Event — Malfunction (MDR 3008114965-2020-00145) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICRUSFRAME10 6MM X 26CM; Generic name: NEUROVASCULAR EMBOLIZATION DEVICE; Manufacturer: MEDOS INTERNATIONAL SARL.
| Device | MICRUSFRAME10 6MM X 26CM |
|---|---|
| Generic name | NEUROVASCULAR EMBOLIZATION DEVICE |
| Manufacturer | MEDOS INTERNATIONAL SARL |
| Report number | 3008114965-2020-00145 |
| Event type | Malfunction |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | PRODUCT COMPLAINT #(B)(4). INFORMATION REGARDING PATIENT WEIGHT, HEIGHT, MEDICAL HISTORY, RACE, AND ETHNICITY WAS NOT REPORTED. PROCODE: KRD/HCG. A SUPPLEMENTAL REPORT WILL BE SUBMITTED IF NEW FACTS ARISE WHICH MATERIALLY ALTER INFORMATION SUBMITTED IN A PREVIOUS MDR REPORT. THIS IS ONE OF THREE PRODUCTS INVOLVED WITH THE COMPLAINT AND THE ASSOCIATED MANUFACTURER REPORT NUMBERS ARE 3008114965-2020 |
| Source | openFDA MAUDE (device adverse events) |
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