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Sterile Filtration (47)
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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High capacity platform for conventional sterile filtration
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< 0.25 EU/mL as determined by the LAL test
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Sartopore® 2 XLG
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All materials of this filter element meet the requirements of the current USP Biological Reactivity tests <88> for plastics Class VI (Systemic Injection, Intracutaneous and Implantation tests).
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