MAUDE manufacturer profile
AESCULAP AG · MDM
MAUDE profile for Instrument, Manual, Surgical, General Use
Key facts
| Manufacturer | AESCULAP AG |
|---|---|
| Manufacturer group | AESCULAP AG |
| Product code | MDM |
| Product code name | Instrument, Manual, Surgical, General Use |
At a glance
- 10–99 MAUDE reports
- 10–99 Injury reports
- 10–99 Malfunction reports
- 10–99 Problems flagged by Orca1 signal analytics
- Break, Detachment Of Device Component, Insufficient Information, No Known Impact Or Consequence To Patient, Foreign Body In Patient, Adverse Event Without Identified Device or Use Problem, Device Embedded In Tissue or Plaque, Failure of Implant 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