U-Pette Blood Drop Dispenser


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.

U-Pette™ is compliant with the IVD regulation 2017/746 and lot tested Endotoxin Free (non-pyrogenic).

Endotoxin 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.
RNase/DNase 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
ATP 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.
BSE/TSE 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.
USP 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.
Prop 65 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 Phthalates & Oleamide
All our resins are medical grade and are certified free of Bisphenol A (BPA), Oleamide, DiHEMDA, and Phthalates.
SVHC 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.
USA Origin
These products are Made in USA and all components meet the requirements for US origin under the NAFTA agreement.
FDA 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.
CE CE Compliant
As applicable Labcon products meet the requirements for CE marking under regulation 2017/746.
ISO 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
Grade Medical
Rating USP Class VI
Colors Natural (Clear)
Fits Most popular blood collection tubes
Approved Use Medical, Clinical, Research
Lot Expiration 4 years
Reclosable Box

Loose pack U-Pette® are supplied in resealable boxes.

FDA Registered

Labcon is registered by the U.S. Food and Drug Administration to manufacture medical devices.

Medical Grade Resins

Only 100% Medical Grade virgin polypropylene resins are used in U-Pette™. No recycled plastics or commodity grade resins.

Lab Tested

U-Pette™ Blood dispensers are developed using our own in-house laboratory. We use actual lab results with real cassettes.

Certified Quality

Our products are made to ISO standards and we are audited every 6 months to ensure you continous quality.

Certificates Online

Real test certificates are available by lot for U-Pette™ for you to download from the certificates page.

Sustainability Built In

U-Pette™ droppers are designed from the beginning with sustainability in mind. Beyond simple recycling to real solutions.