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MDR event

Received Sep 2, 2005 · Event occurred Jul 22, 2005

Report 1221826-2005-00017 · MDR key 633331

Device

Product problems

Material Separation

Patient

Not reported

Burn(s)
Pain

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.