Large Centrifuge Tubes, 175 mL PerformR®, Nonsterile, in Bags, case/48

175 mL PerformR® Centrifuge Tubes, in Bags. Packaged in 24 Bags of 2.

Our large centrifuge tubes give you more performance and convenience than other brands of large centrifuge tubes. Made from a medical grade resin that is far cleaner and durable than commodity grade resins used in most other brands of tubes. This high quality resin is radiation stabilized so you can spin these tubes to 8,000 RCF. PerformR® large format tubes feature our exclusive elastomeric molded-in sealing caps that can be autoclaved. PerformR® large format tubes were designed to give you the convenience of a disposable tube with the performance of a reusable tube.

Specifications

• Conical centrifuge tube
• PerformR®
• Nonsterile
• 175 mL
• With attached flat integral elastomeric seal screw caps, side graduations, and writing surface
• ATP, RNase/DNase and Endotoxin Free (non-pyrogenic)
• Polypropylene USP Class VI resin
• Centrifuging to 8,000 x G
• Freezable to -80C
• Autoclavable
• Capacity: 175 mL
• Teal color caps
• 2 per bag/24 bags per case
• 61mm W. 137mm H.
• Made in USA

	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.
	Heavy Metals Free Heavy metals have been tested for using the prescribed USP method and confirmed to have levels lower than 1 part per million (1ppm)
	Validated Sterilization Labcon products are sterilized by radiation sterilization within a dose range of 12-35 kGy. The dose range necessary for the stated sterility assurance level is continuously audited through quarterly bio-burden and sterility validation studies performed according to the ANSI/AAMI/ISO 11137 standard by an independent laboratory. This dosage is sufficient to guarantee a sterility assurance level of 10-6.

	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 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.
	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.