MAUDE report
MAUDE report 27890: SERIES 10,000 UNIPAK WITH UDS
Malfunction · received Nov 6, 1995 · ALCON SURGICAL, ALCON LABS, INC.
Key facts
| MDR report key | 27890 |
|---|---|
| Report number | MW1007587 |
| Event type | Malfunction |
| Brand name | SERIES 10,000 UNIPAK WITH UDS |
| Model number | 316-1214-777 |
| Catalog number | 316-1214-777 |
| Manufacturer | ALCON SURGICAL, ALCON LABS, INC. |
| Product code | HQE |
| Device class | Class II |
| Date received by FDA | Nov 6, 1995 |
| Report date | Oct 30, 1995 |
| Report source | Maude |
At a glance
- None Device problems coded
- 1,000+ MAUDE reports for this product code
- 1–9 MAUDE reports for this brand
- None Death reports for this brand
- None Injury reports for this brand
- No Adverse event flagged
- Yes Product problem flagged
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About MAUDE medical device reports
MAUDE holds medical device reports (MDRs) of suspected device-associated deaths, serious injuries and malfunctions submitted to the FDA by manufacturers, importers, user facilities and the public. A report alone does not establish that a device caused an event.
Source: U.S. Food and Drug Administration (FDA), MAUDE (Manufacturer and User Facility Device Experience) database · Source date: