FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model OP6581 · UDI-DI 10885403099878

HNI Prescription
2
510(k) clearances
27
Adverse events
0
Recalls
159
Facilities

Description

V. Mueller RIZZUTI IRIS RETRACTOR AND EXPRESSOR RETRACTOR 2.5MM WIDE MALLEABLE SHAFT

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 docs
Data 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.