FDA Device Intelligence
HomeKarl Storz GmbH & Co. KG › CLICKLINE

CLICKLINE

Karl Storz GmbH & Co. KG · Model 26410M · UDI-DI 04048551426845

NWW Prescription
0
510(k) clearances
66
Adverse events (1 deaths)
0
Recalls
58
Facilities

Description

CLICKLINE Outer Sheath

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.