Fresenius Medical Care North America
FRESENIUS COMBILINES LOW VOLUME BLOOD TUBING SET, MODELS 03-2291 (POST PUMP) AND 03-2292 (PRE-PUMP)
SKU K001107UPC FJK
In Stock
—
IIFDA 510(k) Cleared (K001107)
1
Free shipping on orders over $99 · 30-day returns
Healix Assistant
Ask me anything about our products
Quick questions
Powered by Healix AI · Talk to a human
Fresenius Medical Care North America
Free shipping on orders over $99 · 30-day returns
FRESENIUS COMBILINES LOW VOLUME BLOOD TUBING SET, MODELS 03-2291 (POST PUMP) AND 03-2292 (PRE-PUMP) is an FDA 510(k)-cleared medical device (K001107) manufactured by Fresenius Medical Care North America. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 22, 2000. Regulation: 8.
Coloplast
SKU MSC612995
Karl Storz Endoscopy
SKU K942112
Coloplast
SKU MSC750215
Coloplast
SKU MSC891872