FDA Device Intelligence
HomeMIDMARK CORPORATION › Midmark

Midmark

MIDMARK CORPORATION · Model 9A427001 · UDI-DI 00841709110993

GBB
8
510(k) clearances
90
Adverse events (1 deaths)
1
Recalls
45
Facilities

Description

The Midmark fixed top swing arm instrument tray is designed to allow for the placement of instruments and supplies within easy reach, close to the patient, and attaches to the chair to save floor space.

Recalls

DateFirmReason
2014-11-14TransMotion Medical IncThe firm is finding that the stretcher chair controllers are moving the chairs involuntarily.

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.