FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model OS8149-56 · UDI-DI 10885403160189

GFI Prescription
6
510(k) clearances
61
Adverse events
0
Recalls
145
Facilities

Description

V. Mueller CHISEL SYSTEM WITH HANDLE AND 3 BLADES

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.