FDA Device Intelligence
Home › NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. › AED

AED

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Model 32-4410 · UDI-DI 00848657020985

EZO Prescription
5
510(k) clearances
69
Adverse events
1
Recalls
37
Facilities

Description

AED Dittel Bougies straight without channel 22.5 CH

Recalls

DateFirmReason
2010-12-22Olympus America Inc.The device sterile package seal shows evidence of being breached or was breached

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 docs
Data 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.