MAUDE manufacturer profile
VERICEL · OCE
MAUDE profile for Cultured Epithelial Autograft
Key facts
| Manufacturer | VERICEL |
|---|---|
| Manufacturer group | VERICEL |
| Product code | OCE |
| Product code name | Cultured Epithelial Autograft |
At a glance
- 10–99 MAUDE reports
- 10–99 Death reports
- 1–9 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Adverse Event Without Identified Device or Use Problem, Death, Appropriate Term / Code Not Available, Fluid/Blood Leak, No Clinical Signs, Symptoms or Conditions, Multiple Organ Dysfunction Syndrome, Insufficient Information, Mechanical Problem 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