Cannula, For Tracheostomy, With Cuff Number 8, 0, Disposable, Sterile, Pvc, Siliconized, Transparent, Jammed, Composed Of External Cannula With Low Pressure Balloon, Opaque Cuff, Rotator Connector, Round -Tipped And Easy Handling, Radiopaca Line Continuous, Attraumatic Plot, Wings For Fixing With Printing Number In Visible Place And With Canula Fixing Ribbor. Individual Input, In Role Surgical Degree And Thermoplastic Film, Opening In Petala. In The Packaging Should Be Printed Identification Data, Procedure, Manufacturing Date, Type Of Sterilization, Shelf Life And Registration In The Ministry Of Health, Mask, For Oxygen Therapy, Soft And Transparent Vinyl Facilitating Visual Evaluation, With Adjustable Nose Clip For Comfortable Fixation, Visual Track With Adjustable Nose Clip, Adjustable Elastic Track Face Of The Patient, Low Resistance Control Valve, Preventing Gases Reinalalation And The Second Membrane Of The Mask Allowing The Exhaled Gas To Eliminate. Complete System With 750Ml Capacity Reserve Scholarship And 2, 10M Long Oxygen Supply Pipe, Standard Connector, Allowing Therapy Up To 100%O2, Adult Size. Brand With Product Identification, Manufacturer Brand, Soft And Transparent Vinyl Manufacturing Date, Facilitating Visual Assessment With Adjustable Nose To Comply For Comfortable Fixation, Previnating Gas Reinalization And The Second Membrane In The Mask Allowing The Alim About Exhaled Gas. Security Opening Allowing Ambient Air Inlet, Complete System With 750Ml Capacity Reserve Scholarship And 2 Oxygen Supply Tube, Standard Connector, Allowing Up To 100% O2 Therapy, Pediatric Size With Product Identification Data, Scalpel, With Axic, Apirogenic, Unique Use No. Cable, With Security Protector And Locking System Or Retraction System. It Must Be In Accordance With Nr32. Primary Inbound In Accordance With The Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Asptic, Sterile And Apirogenic Technique; According To Rdc 185/2001; The Label Of The Primary Packaging And/Or The Product Itself Must Contain Product Identification And Characteristics, Such As: Manufacturer Name, Lot, Product Validity, Sterilization Method, Sterilization Validity; Name Of Technical Responsible, Anvisa/Ms Registration; Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Ensure The Integrity Of The Product During Storage Until The Time Of Use; The Product Must Obey, For Disposable Pvc Tracheostomy, Number 6.0, With High Volume Cuff And Low Pressure, Balloon With Leur And Leur-Lock Syringe Connector, Shutter Lid, Attractive Tip And Cannula Fixation Tape. Primary Packaging Packed According To Packaging Standards That Guarantee The Integrity Of The Product Until The Moment Of Its Use, Allowing Opening And Transfer With Asptic Technique. The Label Of The Primary Packaging And/Or The Product Itself Must Contain Identification Information And Characteristics Of The Product, Record Anvisa/Ms. The Secondary Packaging Should Be According To The Manufacturers Usual, In Order To Guarantee
