<Genx> Intl., Inc.
<GENX> SINGLE LUMEN SIDEPORT NEEDLE
SKU K991264UPC MQE
In Stock
—
IIFDA 510(k) Cleared (K991264)
1
Free shipping on orders over $99 · 30-day returns
<Genx> Intl., Inc.
Free shipping on orders over $99 · 30-day returns
<GENX> SINGLE LUMEN SIDEPORT NEEDLE is an FDA 510(k)-cleared medical device (K991264) manufactured by <Genx> Intl., Inc.. 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 8, 1999. Regulation: 8.
Ansell
SKU MSC846624
Princeton BioMeditech Corp.
SKU K014192
McKesson
SKU VM-1270030
Hollister
SKU VM-1270031