MAUDE manufacturer profile
ABBOTT MEDICAL · KRD
MAUDE profile for Device, Vascular, For Promoting Embolization
Key facts
| Manufacturer | ABBOTT MEDICAL |
|---|---|
| Manufacturer group | ABBOTT MEDICAL REG# 2135147 |
| Product code | KRD |
| Product code name | Device, Vascular, For Promoting Embolization |
At a glance
- 100–999 MAUDE reports
- 10–99 Death reports
- 100–999 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Clinical Signs, Symptoms or Conditions, Migration or Expulsion of Device, Off-Label Use, Adverse Event Without Identified Device or Use Problem, Patient Device Interaction Problem, Difficult to Fold, Unfold or Collapse, Obstruction/Occlusion, Insufficient Information Most reported problems
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE manufacturer and product code profiles
Manufacturer profiles aggregate MAUDE reports for one manufacturer within one product code, the level at which device safety signals are usually reviewed.
Source: U.S. Food and Drug Administration (FDA), MAUDE database; aggregation by Orca1