Home › DX PRODUCTS LIMITED › VAXAID
VAXAID
DX PRODUCTS LIMITED · Model V3 DELUXE · UDI-DI 05060140200895
10
510(k) clearances
17
Adverse events
0
Recalls
48
Facilities
Description
Vaxaid V3 Deluxe
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.
