Hollow Fiber Filtration
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Renaflo® II Hemofilters
From the
Hemofiltration Specialists
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Biocompatibility
- Polysulfone membrane offers
excellent biocompatibility
- Meets the biocompatibility requirements
of ISO 10993-4 selection of tests, for
interactions with blood
- No anaphylactic responses
reported with the
Renaflo II hemofilters
Convenience
- No-rinse fiber offers
convenient setup
- Complete model selection provides
ultrafiltration rates for the full range
of patients from the neonate to the
largest adult
Reliability / Safety
- Proprietary fiber-manufacturing process
ensures consistent performance
- Hollow fibers used in Renaflo II are
proven to remove small and mediumsized
solutes such as IL-6, TNFa, C3a,
and C5a from the vascular space while
conserving the cellular elements and
proteins in the circulating blood
- Manufactured under
U.S. Patent 5,762,798
The Renaflo® II Familiy
The Renaflo II HF hemofilters are designed
using glycerine-free polysulfone membranes.
These membranes have exceptional
biocompatibility for a broad range of medical
device applications. Their superior blood
compatibility is well documented with
clinical evidence.1,2
Minntech’s expertise and knowledge,
accumulated from over 35 years of development,
manufacturing and clinical experience,
is reflected in the quality and innovation
of the Renaflo® II family.
References
| 1 |
Kramer, P., Wigger, W., Rieger, J., Matthaei, D., Scheler, F., Arteriovenous Hemofiltration: A new and simple method for treatment
of overhydrated patients resistant to diuretics. Klin. Wachr. 55:1121-2, 1977 |
| 2 |
Kaplan, A.A., Longnecker, R. E., and Folkert, V.W., Continuous Arteriovenous Hemofiltration: A report of six month’s experience.
Ann. Intern. Med. 100:358-67, 1984 |
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