MAUDE manufacturer profile
CORDIS DE MEXICO · DQY
MAUDE profile for Catheter, Percutaneous
Key facts
| Manufacturer | CORDIS DE MEXICO |
|---|---|
| Manufacturer group | CORDIS CORPORATION |
| Product code | DQY |
| Product code name | Catheter, Percutaneous |
At a glance
- 100–999 MAUDE reports
- 1–9 Death reports
- 100–999 Injury reports
- 100–999 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- No Consequences Or Impact To Patient, Detachment Of Device Component, Crack, Unsealed Device Packaging, Adverse Event Without Identified Device or Use Problem, Difficult to Insert, Physical Resistance, Delivered as Unsterile Product 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