Falcon™ Pipets, Serol Triple Bagged, Plastic/Plastic, Sterile, Bulk

Description

Corning’s triple-bagged packaged pipets are a safety and convenience revolution. This packaging protects the product from external contamination and is ideal for laboratory clean rooms, such as cell-based vaccine or drug production facilities.

• Triple-bagged in two outer bags
• Manufactured and packaged with animal-free materials
• Sterility Assurance Level (SAL) of 10^-6
• USP Class VI tested
• Nonpyrogenic
• Noncytotoxic
• RNase-/DNase-free
• Human DNA-free
• Low particulate according to USP 788
• Extractables data available upon request
• Color-coded magnifier stripes make volume reading and size selection easier
• Bidirectional graduations provide choice of ascending and descending scales
• Negative graduations allow additional working volume
• Each pipet is individually wrapped in easy open plastic
• No need for decontamination spraying with alcohol
• Manufactured in USA

Specifications

• Material: Plastic
• Sterility: Sterile
• Graduations: Yes
• Quantity: 1000/Pk.
• Packaging Type: Triple Bagged, Bulk
• Color: Transparent
• Volume (Metric): 1 mL
• Type: Serological Pipet
• Disposable: Reusable

Unless otherwise specified, all products are for research use or general laboratory use only. Not intended for use in diagnostic or therapeutic procedures. Not for use in humans. These products are not intended to mitigate the presence of microorganisms on surfaces or in the environment, where such organisms can be deleterious to humans or the environment. Corning Life Sciences makes no claims regarding the performance of these products for clinical or diagnostic applications.

Corning's products are not specifically designed and tested for diagnostic testing. Many Corning products, though not specific for diagnostic testing, can be used in the workflow and preparation of the test at the customers discretion. Customers may use these products to support their claims. We cannot make any claims or statements that our products are approved for diagnostic testing either directly or indirectly. The customer is responsible for any testing, validation, and/or regulatory submissions that may be required to support the safety and efficacy of their intended application.