
M.D. Intl., Inc.
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DMI SERIES 90 EXAMINATION TABLE is an FDA 510(k)-cleared medical device (K894788) manufactured by M.D. Intl., Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 7, 1989. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031