FDA Device Intelligence
Home › STERIS › NA

NA

STERIS · Model Table Pad · UDI-DI 00724995169534

LWG
4
510(k) clearances
36
Adverse events
1
Recalls
59
Facilities

Description

Welded Seam 2-inch Cushion is used with the CMAX X-Ray Image-Guided Table

Recalls

DateFirmReason
2016-04-19Berchtold Corp.The Surgical Table Cushion (HybriGel Pads) could potentially contain staples that's secure two underlying fabrics, which would be captured on certain scans on patients, such as x-r

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.