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GRI Medical & Electronic Technology Co., Ltd. · Model APS005 · UDI-DI 16931918170749
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510(k) clearances
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Adverse events
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Recalls
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Facilities
Description
D & C Pack_Sterile_3EA/CS
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.
