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Allergic reactions to latex, or natural rubbers, is a health risk. NNI takes
such a risk seriously, and has taken measures to make sure that our products do
not contain these compounds. The FDA requires labeling of medical devices that
contain latex or natural rubber, 21CFR section 801.437.
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In compliance with the United States Food & Drug Administration (FDA)
regulations published in the Code of Federal Regulations (CFR), Title 21, §
801.437 "User labeling for devices that contain natural rubber", this is to
document that NALGENE® brand products and packaging do not contain any:
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Natural rubber latex, or
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Dry natural rubber, or
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Synthetic latex or synthetic rubber that contains natural rubber in its
formulation.
The only exception is the Filter Stopper, catalog number DS0396-0080 (Filter
stopper, No. 8, rubber). This product is also a component supplied with the
Filter Funnel with Clamp, catalog number 315-0047, and the Microbiological
Monitors, catalog numbers 136-4547, 136-4556, 137-4547 and 137-4556. It should
be noted that these products are not listed as medical devices.
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