Pentair
39 catalogue numbers from 345280000, listed by Pentair Filtration Solutions, United States, under Filter, Prebypass, Cardiopulmonary Bypass. 1 manufacturer in China is registered for this product code.
Filter, Prebypass, Cardiopulmonary Bypass
Who Makes This Device Type in China?
The one Chinese manufacturer registered for this device type is based in Zhejiang.
- Zhejiang Mediunion Healthcare Group Co., Ltd. Zhejiang, contract manufacturer
How Is KRJ Classified?
Filter, Prebypass, Cardiopulmonary Bypass is FDA product code KRJ, Class 2, 21 CFR 870.4280.
What Does It Take to Sell It in the United States?
It is exempt from premarket notification: the manufacturer registers its establishment and lists the device, and no 510(k) is needed before it is sold in the United States.
Name
Record