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Aortic Stent

FDA product code PNF · Class 3 · Unknown

309

Registered devices

91

Adverse events

0

Recalls

0

510(k) clearances

Devices with this code

G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC NuDEL — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC NuDEL — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC G-ARMOR STENT® — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC CP Stent™ — B BRAUN INTERVENTIONAL SYSTEMS, INC

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.