Query: What are the parameters you use for documenting, intraoperatively, the meds/devices used during a procedure?
Ex: Cryolife Bioglue, Genzyme FocalSeal, sterile talc, hemostatic agents, etc.
Some product literature indicates they are devices and others are medications.
What does your facility do to document the use of such products?
We have two areas of documentation:1)the implant record 2) the intraop medication reocrd.