馃嚭馃嚫Regulatoryopen.fda.govTier 1 路 Regulatory source
Device recall: 5008X Blood Tubing Set, 24 units per case. Includes the below model numbers and descriptions. 1. 5008X HD Pre-Flush Standard Blood Tubing Set; Model Number: 03-5110-6. 2. 5008X HD Pre-Flush With Twister Blood Tubing Set; Model Number: 03-5160-1. 3. 5008X HD/HDF Standard Blood Tubing S
Official structured record identifier: 99061.
openFDA Device RecallsOriginal source






