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Nano-CheckTM DAT 10M
NANO-DITECH CORPORATION · Model AD101U · UDI-DI 00895160002144
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510(k) clearances
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Adverse events
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Recalls
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Facilities
Description
In Vitro Diagnostic Test kit for the detection of Multi-Drugs in human urine.
Query this across every FDA database — by API.
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.
