Home › AMBLER SURGICAL CORP. › Ambler Surgical
Ambler Surgical
AMBLER SURGICAL CORP. · Model Outer sheath · UDI-DI 00190660173531
FBM
Prescription
9
510(k) clearances
20
Adverse events
0
Recalls
51
Facilities
Description
Outer sheath, insulated, 5.0mm diameter, 210.0mm working length
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.
