AseptiCap® NL/NS Small
MDI AseptiCap NL/NS Nylon 66 membrane capsule filters are sterilizing grade filters offering absolute retention, wide chemical compatibility, and very low hold up volumes.
- Single Layered: AseptiCap NL
- Multiple Layered:AseptiCap NS
| Consistent and Reliable Quality: | AseptiCap capsule filters are produced with ISO 9001 certified quality management systems. |
| Regulatory Compliance: | Meet all pharmacopeial and compendia requirements and are registered with USFDA DMF #015554 |
| Total traceability: | Unique marking on each filter |
- Sterilizing filtration of stability batches in formulation development tabs.
- Sterilization of Compatible solvents and chemicals.
| Construction | |||||
| Membrane | Nylon 66 | ||||
| Final Filter Pore Size |
|
||||
| Support Layers | Polyester | ||||
| Body and Core | Polypropylene | ||||
| Prefilter Pore Size (In case of AseptiCap NS) |
|
||||
| Size | |||||
| Size |
|
||||
| Effective Filtration Area (Nominal) – AseptiCap NL |
|
||||
| Dimension (End to End) – 1½” Sanitary Flange Inlet ½” Single Step Hose Barb Outlet |
|
||||
| Effective Filtration Area (Nominal) – AseptiCap NS |
|
||||
| Dimension (End to End) – ¾” Sanitary Flange Inlet I/O |
|
||||
| Dimension (End to End) – 1½” Sanitary Flange I/O |
|
||||
| Dimension (End to End) – ½” Hose Barb I/O |
|
||||
| Dimension (End to End) – ½” Single Step Hose Barb I/O |
|
||||
| Operational Radius (with Vent/ Drain) |
|
||||
| Vent and Drain |
|
||||
| Integrity Testing / Retention | |||||
| Microbial Retention |
|
||||
| Bubble Point (with 50% IPA) |
|
||||
| Operational | |||||
| Max. Operating Temperature | 80 °C @ < 30 psi (2 Kg/cm²) | ||||
| Max. Differential Pressure | < 60 psi (4 Kg/cm²) @ 30 °C | ||||
| Sterilization By Gas | Sterilizable by Ethylene Oxide | ||||
| Sterilization By Autoclave | Autoclavable at 125 °C for 30 minutes and it cannot be in-line steam sterilized. | ||||
| Shelf Life | 3 years after EO sterilization | ||||
| Assurance | |||||
| Toxicity | Passes Bioreactivity test, In Vivo, as per USP <88> for Class VI plastics | ||||
| Bacterial Endotoxin | Aqueous extracts exhibit < 0.25 EU/ml as established by Limulus Amebocyte Lysate (LAL) Test | ||||
| Bioburden | Bioburden level is < 1000 cfu/filter device as per ISO 11737-1 : 2018 | ||||
| Non Fiber Releasing | Passes test as per USP and comply with USFDA 21 CFR Part 210.3(b)(3) for fiber release | ||||
| Indirect Food Additive | All Polypropylene components meet the FDA Indirect Food Additive requirements cited in 21 CFR 177.1520 | ||||
| Extractables with WFI | Passes NVR test as per USP <661> | ||||
| Good Manufacturing Practice | These products are manufactured in a facility which adheres to Good Manufacturing Practices. | ||||
| Oxidizable Substances | Within limits as specified in USP <1231> | ||||
| Particle Shedding | Passes USP test for particulates in injectables. | ||||
| TOC/Conductivity at 25 °C | Meets the WFI requirements of USP <643> for Total Organic Carbon and USP <645> for Water Conductivity after a 3 liter of WFI flush | ||||
| Quality Management System | ISO-9001 Certified | ||||
| USFDA | DMF No. 015554 | ||||
|
|
|
|
|
|
|
|
||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
*0.45μm Upstream is only available in 0.2μm Pore Size
**1” Capsule Filters are not available with ½” Single step Hose Barb and ½” MNPT
***3/16″ Hose Barb end connection is available in:
- 1″ and 2″ capsule filters as inlet and outlet
- 5″ capsule filters as outlet only
****Male luer slip is available only in 1” capsule filter as outlet
*****Bell is available with:
- ½” Hose Barb outlet connections in 1″, 2″, 5″ and 8″ capsule filters
- ¼” SHB outlet connection in 1″ capsule filters only
Example :
| DNS5 | 52 | 01 | DD | X | X | 1 | 01 |
Example for Non Sterile: DNS55201DDXX101 Example for EO Sterile: DNS55201DDXX201
Have questions or need assistance?
Our team is here to help! Contact us today, and we’ll get back to you as soon as possible.