FDA Device Intelligence
Home › CENTRIX, INC. › Accudose

Accudose

CENTRIX, INC. · Model 290038 · UDI-DI 00817051022277

EIY Prescription
5
510(k) clearances
18
Adverse events
0
Recalls
187
Facilities

Description

SofNeedle 22 ga Tip

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.