Bids Are Invited For Price Registration To Hire A Company For The Possible Supply Of Blood Glucose Test Strips In View Of The Demand For Supply For Diabetic And/Or Insulin-Dependent Patients, In Support Of The Family Health Strategy Units.

Reagent Strip For Quantitative Blood Glucose Determination. Sample Of Fresh Capillary, Venous, Arterial And Neonatal Blood And Also Capillary Blood From Newborns, Children, Adults And Patients Using Vasoactive Drugs, As Well As Patients In Icu, Which May Be Subject To Variations In Results Predicted And Acceptable By Technical Standard Iso 15.197/2013. Use Of A Compatible Blood Glucose Monitor; Measuring Range From 10-20 To 500-600Mg/Dl; Amperometric Or Photometric Reading Methodology Using Glucose Dehydrogenase Enzyme (To Minimize The Action Of Interfering Substances); Hematocrit Range Between 20% And 65%, For Safe Measurements In Neonates And Pregnant Women. Storage Temperature 5-25°C; Individual Packaging Or In A Bottle (Containing 50 Or 100 Units), Provided That The Validity Of The Product After Opening Is Guaranteed, In Material That Guarantees The Integrity Of The Product; Labeling Must Contain The Batch Number And Expiration Date Present On The Packaging; Additional Features: Guarantee Of Supply Of One Glucometer For Every 300 Strips On A Lending Basis, Healthcare Professional Responsible For Training And Training In The Use Of The Equipment. Certification: Good Manufacturing Practices Manual, Legislation In Accordance With Current Legislation: Iso 15197-2013. Supply Unit According To Anvisas Registration Unit. Note: 100 Sets Of Devices (Glycometer And Batteries) Must Be Supplied At The Time Of The First Delivery Of The Tapes, On A Lending Basis, And More Devices According To Demand At The Time Of Deliveries And Prior Training For Users. The Proportion Should Be One Set For 300 Tapes. Whenever There Are Problems In Operation, The Devices Must Be Replaced While Tapes Are Available In Stock., Lancets - Single-Use Puncture System, With T-Type External Activator (More Ergonomic), Sterilized By Gamma Radiation; Retractable Safety System, Meeting The Requirements Of Nr-32, Which Prevents Reuse, Avoiding Accidents And/Or Contamination. Devera Unique System With Automatic Needle Retraction Device, Three-Faceted Stainless Steel Needle, Model 26G To 28G, With A Depth Of 1.6Mm Or 1.8Mm, Must Comply With The Standards Established By The Ministry Of Health And Anvisa And Comply With The Requirements As Per Nr. 32. The Material Must Present On The Outside Of The Packaging Manufacturing, Origin And Expiration Data. 1 -- The Product Presentation Must Contain 50 Or 100 Units Per Package.