FDA Device Intelligence
Home › STERIS CORPORATION › V. Mueller

V. Mueller

STERIS CORPORATION · Model RH2000 · UDI-DI 10885403113659

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

Description

DIAMOND RASP SET OF 4 PATTERNS, CVD and STR COARSE GRIT,CVD and STR MED GRIT OVERALL LENGTH 7-1/4 inches18.4CM

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.