FDA Device Intelligence
Home › HANS RUDOLPH, INC. › 9064 MOUTHPIECE

9064 MOUTHPIECE

HANS RUDOLPH, INC. · Model 9064 · UDI-DI 00874750004133

BYP Prescription
10
510(k) clearances
11
Adverse events (1 deaths)
0
Recalls
165
Facilities

Description

MPC SM W/SALIVA TRAP MATE 22MM

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.