
Gynetech Pty. , Ltd.
Free shipping on orders over $99 · 30-day returns
MANIPULATOR; MANIPULATOR PRO is an FDA 510(k)-cleared medical device (K142164) manufactured by Gynetech Pty. , Ltd.. This device is classified under the Obstetrics/Gynecology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 16, 2014. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

McKesson
SKU VM-1270030

Hollister
SKU VM-1270031