Centrifuge Tubes, 50mL with Filtrox® Filtrospin Filter, SuperClear® Polypropylene, case/10

SuperClear® 50mL Tubes with Filtrox® Filtrospin 20 inserts. SuperClear® tubes with FILTROX® PURASPIN® is an ultra high performance centrifuge tube and cap combination that includes a removable FILTROX® funnel insert. The funnel insert includes a FILTROX® filter medium available in various formats and a nozzle that can be fitted to a luer locking syringe or hose. The cap keeps the FILTROX® spinner securely in place with its unique elastomeric seal. The entire assembly forms a neat package that can be disposed of after use. Both the tube, cap, and spinner are made of USP Class VI resin.

Specifications

• Conical centrifuge tube
• SuperClear®
• 50 mL
• With Filtrox® Filtrospin 20 insert
• Polypropylene USP Class VI resin
• Centrifuge to 4,000 x G
• Freezable to -80C
• Not Autoclavable
• Capacity: 20 mL
• Teal color caps
• 10 tubes per box/1 box per case
• 29 mm W. 115 mm H.
• Made in USA and Switzerland

Retention Rates:

• Coarse 10-30µM: Coarse particle filtration with flow rate of 1500 - 2100 liters per square meter.
• Clarifying 5-12µM: Clarifying particle filtration with flow rate of 280 - 360 liters per square meter.
• Fine 1.5-3µM: Fine particle filtration with flow rate of 170- 210 liters per square meter.
• Fine 0.6-1.5µM: Fine particle filtration with flow rate of 98-121 liters per square meter.
• Sterile* 0.4-0.6µM: Sterile particle filtration with flow rate of 43-52 liters per square meter.
• Sterile* 0.1-0.3µM: Sterile filtration with flow rate of 19-29 liters per square meter.

* Product performs a sterilizing function, but has not been sterilized.

Testing

	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.

Certifications

	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.
	Origin These products are Made in USA and Switzerland and components meet the requirements for US origin under the USMCA agreement.

Registrations

	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 Compliant As applicable Labcon products meet the requirements for CE marking under regulation 2017/746.
	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.