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BioPlex 2200

BIO-RAD LABORATORIES, INC. · Model 6651360G · UDI-DI 00847865011341

LJNKTN
10
510(k) clearances
2
Adverse events
0
Recalls
10
Facilities

Description

Manual & CDs, EBV IgM IFU, SW4.1_v1

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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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.