U-Pette™ Multi Drop Dispenser for Blood Collection Tubes
The U-Pette™ makes delivering sample into test cards and point of care cassettes simple and efficient. Since you don't have to open the primary sample tube any risk of exposure to biohazards is eliminated. And no glass capillary tubes means no potential for breakage near your patient. U-Pette™ is ideal for use with any point of care analyzer that uses a separate cassette or test card. Portable analyzers like the Abbott® i-Stat® Helena® Abrazo® and others. You can use the U-Pette™ with any analyzer that requires one or more drops of blood.
Safe Point of Care Testing
U-Pette™ helps enhance point of care testing. It reduces the tedious job of dispensing into analyzer cassettes. Simple to use at patient bedside, the U-Pette™ precisely delivers multiple drops of blood from standard blood collection tubes. Available in boxes of 100. Non sterile and not autoclavable.
The U-Pette® blood collection tube dispenser attaches to most popular brands of blood collection tubes. Once inserted into the stopper they allow you to dispense drops of blood onto test strips or analyzer cassettes.
U-Pette® blood dispensers fit all standard 13mm and 16mm blood collection tubes. Simply insert, invert, and dispense one droplet. The simple intuitive design makes U-Pette™ the best choice for point of care testing cartridges. No special training, no special fittings or inserters. Available in resealable packages of 100..
|Endotoxin Free (Non pyrogenic)
Product samples are exposed to endotoxin-free water and the resulting extraction fluid is tested for contamination using the kinetic turbidimetric Limulus Amoebocyte Lysate (LAL) assay protocol and USP guidelines. All products tested must display less than 0.05 EU/ml to be certified free of endotoxin.
|Nuclease Free (RNase/DNase)
Product samples are exposed to nuclease-free water and the resulting extraction fluid is tested for nuclease activity on commercially available 7.5 kb Poly(A) tailed RNA (1µg) and HindIII-digested DNA (1µg) with a one hour 37°C incubation in appropriate buffers. Results are visualized on an agarose gel with appropriate positive and negative controls. Extraction fluid samples must show no degradation of the nucleic acids by the extraction fluid has occurred for the product to be certified as RNase-free and DNase-free
|Adenosine Triphosphate (ATP)
Product sample surfaces are tested for the presence of adenosine triphosphate (ATP) using a controlled bioluminescence reaction to detect contamination. Luminescence data is compared to results generated by ATP-free surfaces and surfaces with known amounts of ATP as a positive control. The relative light units result must indicate less than 2 X 10-12 mg/µl of ATP for the product to be certified as ATP free.
|Bovine Spongiform Encephalopathy-Transmissible Spongiform Encephalopathy
These products contain resins that are processed under conditions proven to exceed the European Union standard as listed in the 22nd Commission Directive EC 98/16/EC of March 5th, 1998 as annexed to council Directive EC 76/768/EEC and further Amendment 419 Annex II of 12 June 2001.
|Medical Grade (USP)
U.S Pharmacoepia Methods and Guidelines (U.S.P Class VI) are used if applicable. We only use medical grade resins and pre-test all resins for contaminants prior to use. Resins are compliant with FDA CFR title 21-177.1520, 178.3295, 178.3297.
|California Prop 65
No Labcon manufactured disposables contain any of the “listed chemicals” as referenced in the California Safe Drinking Water and Toxic Enforcement Act of 1986, (Prop 65) as revised May 25, 2018.
|Phthalates & Oleamide
All our resins are medical grade and are certified free of Bisphenol A (BPA), Oleamide, DiHEMDA, and Phthalates.
|Substances of Very High Concern & REACH
All Labcon products are compliant with RoHS Directive 2002/95/EC/-2011/65-2015/863, are free of Substances of Very High Concern (SVHC), and are EU REACH Regulation (EC) No 1907/2006 compliant.
These products are Made in USA and all components meet the requirements for US origin under the NAFTA agreement.
|U.S. FDA Registered
Labcon is a U.S. FDA registered medical device manufacturer. Our facility is registered by the U.S. government to comply with CFR21 GMP regulations for manufacturing medical devices.
As applicable Labcon products meet the requirements for CE marking under directive 98/79EEC.
|ISO 9001 Quality Registration
Labcon has been registered to the ISO 9001 quality management system standar since 1997 and maintains registration to ISO 9001:2015.
|Material||100% Virgin Polystyrene|
|Rating||USP Class VI|
|Fits||Most popular blood collection tubes|
|Approved Use||Medical, Clinical, Research|
|Lot Expiration||4 years|