
Schering Research
Free shipping on orders over $99 · 30-day returns
GENTLEHALER(R) is an FDA 510(k)-cleared medical device (K892117) manufactured by Schering Research. This device is classified under the Anesthesiology specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 22, 1989. Regulation: 8.

ADC
SKU DX606933

MDF
SKU DX683863

3M Littmann
SKU DX771242

Welch Allyn
SKU DX297280