FDA Device Intelligence
Home › OLYMPUS Winter & Ibe GmbH › Olympus

Olympus

OLYMPUS Winter & Ibe GmbH · Model A22091A · UDI-DI 04042761021210

FDC Prescription
1
510(k) clearances
442
Adverse events (2 deaths)
0
Recalls
37
Facilities

Description

Working insert, 24 Fr., 6 Fr. channel

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.