Ferrous Sulfate, Oral Solution 25Mg/Ml Fe( Ii ) Fr.30Ml, The Packaging Must Contain The Print Prohibited For Sale By Commerce. Present Registration Of Products With Anvisa And Certificate Of Good Practices, Manufacturing And Control - Cbpfc Of The Manufacturer In Accordance With Anvisa Resolution No. 460/99. In The Case Of A Manufacturer Outside Mercosur, Present A Document From The Country Of Origin Translated By An Official Translator, Propofol, Injectable Emulsion 10 Mg/Ml F.A. 100 Ml (R). The Packaging Must Contain Sales Prohibited By Commerce. Present Registration Of Products With Anvisa And Certificate Of Good Practices, Present Document From The Country Of Origin Translated By An Official Translator., Solution, Glyco-Physiological 1:1 (Glucose 5%+ Chlor. Sodium 0 , 9%) 500Ml, Injectable Solution F.A./Pouch, System Closed. The Packaging Must Contain Commercially Prohibited Sales. Present Product Registration With Anvisa And Certificate Of Good Practices, Manufacturing And Control - Cbpfc From The Manufacturer According To Anvisa Resolution No. 460/99. In The Case Of The Manufacturer Outside Mercosul, Prednisolone, Acetate, 10Mg/Ml Ophthalmic Suspension, Bottle With 5Ml . The Packaging Must Display The Phrase: Sale Prohibited By Commerce. The Supplier Must Present Information Sheet, Product Registration With Anvisa And Certificate Of Good Manufacturing Practices - Cbpf In Compliance With Current Resolutions At Anvisa. If The Manufacturer Is Outside Mercosur, Present A Document From The Country Of Origin Translated By An Official Translator. Supply Unit: Bottle, Umeclidinium, Bromide 62, 5Mcg/Dose + Vilanterol, Trifenatate 25Mcg/Dose, Inhalation Powder, Device With 30 Doses. The Packaging Must Display The Phrase: Sale Prohibited By Commerce. The Supplier Must Present A Leaflet, Product Registration With Anvisa And A Certificate Of Good Manufacturing Practices - Cbpf In Accordance With Current Anvisa Resolutions. If The Manufacturer Is Outside Mercosur, Present A Document From The Country Of Origin Translated By An Official Translator. Unit Of Supply: Device, Injectable Emulsion 10 Mg/Ml F.A. 100 Ml (R). The Packaging Must Contain Commercially Prohibited Sales. Present Product Registration With Anvisa And Certificate Of Good Practices, Product Registration With Anvisa And Certificate Of Good Manufacturing Practices - Cbpf In Accordance With Anvisa Resolutions In Force. In The Case Of The Manufacturer Outside Mercosur
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