cytoQ®

SABEU GmbH & Co. KG · Model cytoQ® Non-Gyn Filters · UDI-DI 04260649292099

510(k) clearances

Adverse events

Recalls

Facilities

Description

Non-sterile, single-use in vitro diagnostic device for preparing biological samples for subsequent diagnostic or analytical procedures. It enables sample collection through filtration from liquid phase in combination with an IVD-certified processor. Designed for clinical use by professionals. cytoQ® Non-Gyn Filters (Blue) are suitable for preparing various non-gynecological cell samples.

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 key Read 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.