What should be included in the label of the whole blood and blood component storage bag (hereinafter referred to as the “blood bag”)?

The label of the blood bag should comply with the requirements of the “ Provisions for Instructions and Labels of Medical Devices”(CFDA Degree No. 6), and should in addition, at least indicate the following: the description of the content and intended use, nominal volume of whole blood and blood components collected, instructions for restriction conditions like sterile and pyrogen-free, instructions for not use if any macroscopically visible signs of deterioration are found, instructions indicating for single use only, batch numbers, intended storage period of whole blood or blood components, etc.

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What Should Be Included In The Label Of The Whole Blood And Blood Component Storage Bag (hereinafter Referred To As The “blood Bag”)?

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