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Hall Breathe

Huizhou Kaiyi Technology Co., Ltd. · Model VIS-05 · UDI-DI 06973280040032

BWF
10
510(k) clearances
192
Adverse events (4 deaths)
1
Recalls
51
Facilities

Recalls

DateFirmReason
2020-12-21Smiths Medical ASD Inc.Shipping box may contain wrong model.

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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.