Search Compliance About

MalfunctionFII

MDR event

Received Jan 22, 2008

Report 9616240-2008-00006 · MDR key 996434

Device

Product problems

Fluid/Blood Leak

Patient

Not reported

No Consequences Or Impact To Patient

inforMED sources data from the FDA's public MAUDE, recall, 510(k), and registration & listing databases via openFDA.

Not affiliated with the FDA. Data is unvalidated and may be incomplete — verify anything decision-critical against the source database.