FDA Device Intelligence
Home › Coopersurgical, Inc. › Uterobrush

Uterobrush

Coopersurgical, Inc. · Model E0001 · UDI-DI 00888937003291

HFE Prescription
1
510(k) clearances
5
Adverse events
1
Recalls
9
Facilities

Description

Endometrial brush

Recalls

DateFirmReason
2009-04-02Cook OB/Gyn, Inc.There is an ink on the brush which has not been tested for use with the Tao Brush.

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.