Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human

Vitrolife Sweden AB
Free shipping on orders over $99 · 30-day returns
G-1 VERSION 3, MODEL 10048 is an FDA 510(k)-cleared medical device (K022244) manufactured by Vitrolife Sweden AB. 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 September 5, 2002. Regulation: 8.

Ansell
SKU MSC846624

Princeton BioMeditech Corp.
SKU K014192

Ohmeda Medical
SKU K871399

Insulet Corporation
SKU K182630