FDA Device Intelligence
HomeSTERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model RH2110-005 · UDI-DI 10885403113963

KBA Prescription
0
510(k) clearances
1
Adverse events
0
Recalls
86
Facilities

Description

V. Mueller DOUBLE-ENDED RASP GRIT 5 and 6, COARSE and COARSE TUNGSTEN CARBIDE ENDS OVERALL LENGTH 8-1/4 inches 21CM

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.