FDA Device Intelligence
Home › MIDMARK CORPORATION › Midmark

Midmark

MIDMARK CORPORATION · Model 9A267003 · UDI-DI 00841709110979

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

Description

The Midmark double arm instrument tray is designed to hold instruments and supplies close to the patient, and it attaches to either side of the chair for flexibility and 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.