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tellihealth

Shenzhen Urion Technology Co., Ltd · Model U30B · UDI-DI 06953825905927

INF
5
510(k) clearances
7
Adverse events (1 deaths)
0
Recalls
30
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.