FDA Device Intelligence
Home › BIO-RAD LABORATORIES, INC. › BioPlex 2200

BioPlex 2200

BIO-RAD LABORATORIES, INC. · Model SW4V2 · UDI-DI 00847865002387

MVJMOB
6
510(k) clearances
3
Adverse events
0
Recalls
13
Facilities

Description

Manual & CDs, BioPlex 2200, Vasculitis IFU, SW4_v2

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.