Copper Iud (Tcu 380A Or Similar High-Efficiency Device) Composition T-Shaped Device Or Similar (Adaptable To The Uterine Cavity), Composed Of A Radiopaque Plastic Body (Polyethylene), Covered With High Purity Copper Wire (Minimum 99.9%). Copper Area Minimum Nominal Active Copper Surface Area Of 380 Mm² (Tcu 380A Or Equivalent), In Accordance With Anvisa Technical Standards. Durability Must Have A Term Of Contraceptive Effectiveness And Continuous Use Declared And Proven By The Manufacturer Of At Least 10 (Ten) Years. Presentation The Iud Must Be Pre-Assembled, Sterile (Sterilized By Gamma Radiation Or Ethylene Oxide) And Individually Packaged In Tamper-Evident Packaging. Insertion Kit The Individual Packaging Must Include The Insertion Tube (Applicator) With Movable Guide (Flange/Depth Marker) And The Other Components Necessary For The Aseptic Insertion Technique (No-Touch). Guide Wire Have A Polyethylene Guide Wire (Removal Wire), In White Or Blue, With Adequate Length And Visible After Insertion. Regulation Active And Valid Registration With Anvisa (National Health Surveillance Agency) And In Compliance With Good Manufacturing Practices (Bpf). Validity On Delivery Minimum Remaining Validity Period Of 12 Months Or 70% Of The Total Term. (Reserved Quota Broad Competition 75%), Subdermal Contraceptive Implant (Etonogestrel 68 Mg) Composition Single Stick, Soft And Flexible, With Approximate Dimensions Of 4 Cm In Length By 2 Mm In Diameter. Active Ingredient Containing 68 Mg (Milligrams) Of Etonogestrel, As Active Substance. Characteristics The Implant Must Be Radiopaque (Visible On X-Ray) To Facilitate Location And Removal. Must Be Non-Biodegradable. Durability Term Of Contraceptive Effectiveness And Continuous Use Declared And Proven By The Manufacturer Of 3 (Three) Years (Or According To Anvisa Registration). Presentation The Implant Must Be Supplied Pre-Loaded In A Sterile, Disposable Applicator And Ready For Subdermal Use, According To The Manufacturers Specifications. Registration And Regulation Active And Valid Registration With Anvisa (National Health Surveillance Agency) And In Compliance With Good Manufacturing Practices (Bpf). It Must Be A Medicine Standardized By The Ministry Of Health, If Applicable. Individual, Tamper-Proof Packaging, Which Guarantees Sterility And Contains The Leaflet In Portuguese. Validity On Delivery Minimum Remaining Validity Period Of 12 Months Or 70% Of The Total Term. (Reserved Quota Broad Competition 75%), With Suitable Length And Visible After Insertion. Regulation Active And Valid Registration With Anvisa (National Health Surveillance Agency) And In Compliance With Good Manufacturing Practices (Bpf). Validity On Delivery Minimum Remaining Validity Period Of 12 Months Or 70% Of The Total Term. (Exclusive Me/Epp Reserved Quota 25%), Disposable, Sterile, Single-Use Hysterometer Material: Rod Made Of Plastic Material (Polystyrene Or Polypropylene) That Is Malleable, Thin And Flexible, For Greater Comfort And Safety For The Patient And Ease Of Handling By The Professional. Measuring Scale: Centimeter Rod, With Visible Numerical Scale Marking Of At Least 1 Cm To 12 Cm (Or 4 Cm To 15 Cm, According To Standard). Cylindrical Flange/Stop: It Must Have An Adjustable Ring (Flange Or Stopper) That Slides Through The Stem Body To Allow Marking And Precise Measurement Of The Length Of The Uterine Cavity. Tip Diameter: Distal Tip Diameter (Insertion Tip) Cylindrical (Around 4 M
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