Home › Angiomed GmbH & Co. Medizintechnik KG › COVERA
COVERA
Angiomed GmbH & Co. Medizintechnik KG · Model AVFL08080 · UDI-DI 00801741106989
PFV
Prescription
0
510(k) clearances
2,731
Adverse events (31 deaths)
1
Recalls
16
Facilities
Description
COVERA™ Vascular Covered Stent 8 mm x 80 mm (120 cm delivery catheter) (flared)
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2022-12-22 | Bard Peripheral Vascular Inc | An increase in the reported complaint rate for inability to deploy was identified and related to poor slide block bonding. |
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.