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THERMOBIO
Shenzhen Jumper Medical Equipment Co.,Ltd. · Model https://gudid.fda.gov/gudid/resources/images/icons/icon_info_small.png · UDI-DI 06951740540377
0
510(k) clearances
149
Adverse events
0
Recalls
58
Facilities
Description
Pulse Oximeter
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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
Get your free API keyRead the docsData 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.
