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Syva® RapidTest d.a.u.® 10

Siemens Healthcare Diagnostics Inc. · Model 10445363 · UDI-DI 00842768001345

LFI LCM DJR LAG DKE DIS DIO DJG DKN DKZ

510(k) clearances

Adverse events

Recalls

Facilities

Description

Syva® RapidTest d.a.u.® 10 mAMP/OPI/COC/THC/PCP/BZO/BAR/MDN/TCA/AMP

Query this across every FDA database — by API.

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.