FDA Device Intelligence
Home › CERUS CORPORATION › INTERCEPT Blood System for Plasma

INTERCEPT Blood System for Plasma

CERUS CORPORATION · Model INT3130B · UDI-DI 18717953196993

PJF Prescription
0
510(k) clearances
29
Adverse events (8 deaths)
0
Recalls
6
Facilities

Description

INTERCEPT Blood System for Plasma, Plasma (P) Processing Set

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.