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Pulse Oximeter

Shenzhen Viatom Technology Co.,Ltd. · Model S9 · UDI-DI 06934440102809

OCH
0
510(k) clearances
35
Adverse events
0
Recalls
58
Facilities

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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.