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Aladuck405 V100

SBI PHARMACEUTICALS CO., LTD. · Model 220-21 · UDI-DI 04560304635729

NTN

510(k) clearances

273

Adverse events

Recalls

Facilities

Description

Aladuck405 V100

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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.