FDA Device Intelligence
HomeSTERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model 007-01 · UDI-DI 10885403067945

FHO Prescription
10
510(k) clearances
81
Adverse events (2 deaths)
0
Recalls
40
Facilities

Description

V. Mueller VERRES NEEDLE 150MM DISPOSABLE 12/BX

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.