Zhejiang Xinna Medical Device Technology Co., Ltd.
| Payment Terms | L/C, T/T |
| Delivery Time | 15 to 30 days |
| Packaging Details | Roll packaging or standard export carton packaging |
| Product Name | PTFE Membranes with Polypropylene Support |
| Material | PTFE/PP |
| Pore Size | 0.45μm or Custom |
| Width | 10mm to 300mm |
| Wettability | Hydrophobic |
| Flow Rate | High |
| Chemical Resistance | Excellent |
| Filtration Efficiency | Up to 99% |
| Brand Name | No |
| Model Number | XN-PTFE |
| Certification | ISO9001 |
| Place of Origin | China |
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Product Specification
| Payment Terms | L/C, T/T | Delivery Time | 15 to 30 days |
| Packaging Details | Roll packaging or standard export carton packaging | Product Name | PTFE Membranes with Polypropylene Support |
| Material | PTFE/PP | Pore Size | 0.45μm or Custom |
| Width | 10mm to 300mm | Wettability | Hydrophobic |
| Flow Rate | High | Chemical Resistance | Excellent |
| Filtration Efficiency | Up to 99% | Brand Name | No |
| Model Number | XN-PTFE | Certification | ISO9001 |
| Place of Origin | China |
A BI’s (biological indicator) basic structure includes:
- A plastic pipe (housing a spore strip impregnated with heat-resistant spores + a growth medium like tryptic soy broth).
- A perforated cap placed on top of the pipe to allow sterilizing agent (steam) to penetrate the chamber.
- A filter membrane (0.45μm PTFE) sandwiched between the pipe and cap to act as a controlled barrier. The filter serves three critical roles in the BI system: allowing sterilizing agent penetration, preventing contamination and retaining internal contents.
We manufacture and offer 0.45μm PTFE medical-grade filter for biological indicator (BI) container vents in steam sterilization monitoring. This PTFE filter membrane is specially designed for self-contained biological indicators (BIs).
Functionality Breakdown
1. Steam Penetration & Gas Exchange
During sterilization, the autoclave generates pressurized steam. The 0.45µm PTFE filter acts as a selective barrier:
- Gases/Vapors: Steam (water vapor) easily passes through the porous PTFE structure, reaching the spores in the pipe. This ensures the spores are exposed to the same sterilization conditions as the load being sterilized.
- Air/Fumes: After sterilization, trapped air or residual fumes escape through the filter, preventing pressure buildup in the BI.
2. Barrier Protection
- Pre-Sterilization: When the BI is stored, the filter blocks ambient dust, airborne bacteria, and liquid splashes from contaminating the spore strip or growth medium. This is critical because even minor contamination could lead to false-positive results (growth of non-target microbes) during incubation.
- Post-Sterilization: If the cap is accidentally knocked off or mishandled, the filter prevents the spore suspension (now potentially containing live spores if sterilization failed) from leaking out. This protects healthcare workers and laboratory personnel from accidental exposure.
3. Fluid Resistance
While the primary use case involves gases, the hydrophobic PTFE membrane provides limited protection against accidental fluid ingress (e.g., condensate from steam, spills during handling). It will not pass bulk liquids, but allows vapors and gases to flow freely—ideal for the BI’s dynamic environment.
Key Features
| Feature | Specification | Rationale for BI Use |
| Membrane Material | Polytetrafluoroethylene (PTFE) | *Chemical Resistance: Withstands harsh steam sterilization cycles (121–134°C, pressurized) without degrading. Unlike polyester or cellulose filters, PTFE does not react with steam or cleaning agents. *Hydrophobicity: Repels moisture (condensate from steam) to avoid clogging, ensuring consistent gas flow during sterilization. *Mechanical Strength: Durable enough to maintain structural integrity under pressure (autoclave conditions) and handle repeated handling. |
| Pore Size | 0.45 µm | *Balanced Permeability: Large enough to allow rapid steam penetration (critical for uniform exposure of spores to sterilizing conditions) but small enough to: • Retain most bacteria and all spore clusters (spores are 1–2 µm, but clusters are larger). • Block dust, fibers, and other particulates that could contaminate the BI. *Note: Unlike 0.22 µm “sterile” filters, 0.45 µm is intentional here—full sterility is not required. The goal is to control gas exchange, not eliminate all microbes. In fact, the spores inside the BI are meant to survive if sterilization fails! |
| Medical-Grade Quality | Compliant with ISO standards | Ensures biocompatibility (no leachables that inhibit spore germination) and consistency (lot-to-lot reliability for critical validation studies). Medical-grade certification also confirms absence of pyrogens (endotoxins) . |
Comparison to Other Filters
| Filter Type | Pore Size | Material | Suitability for BI Vents |
| Cellulose | 0.22–0.45µm | Plant-based fiber | Poor chemical resistance (degrades in steam); absorbs moisture, leading to clogging and inconsistent flow. Not durable for repeated autoclaving. |
| Polyester (PET) | 0.22–1.0µm | Synthetic polymer | Marginal steam resistance; may shrink or melt at high temps. Less hydrophobic than PTFE, increasing risk of condensation buildup. |
| PVDF | 0.22–0.45µm | Fluoropolymer | Good chemical resistance but less hydrophobic than PTFE. More expensive than PTFE for equivalent performance. |
| PTFE | 0.45µm+ | Fluoropolymer | Optimal choice: Superior steam/chemical resistance, extreme hydrophobicity, and mechanical strength. Widely adopted in medical sterilization validation due to proven reliability. |
Common Misconceptions Clarified
Q: “Why not use a smaller pore size (e.g., 0.22µm)?”
A: A smaller pore would restrict steam flow, leading to uneven exposure of spores to sterilizing conditions. The 0.45µm pore strikes the perfect balance between allowing adequate gas exchange and maintaining a robust barrier against contaminants.
Q: “Does this filter sterilize the BI itself?”
A: No—its role is to enable sterilization of the contents and protect them from external contamination. The actual sterilization is achieved by the autoclave’s steam killing the spores inside the BI. If sterilization fails, the spores will germinate in the growth medium, indicating a problem with the process.
Q:“Can I reuse the filter?”
A: Most medical-grade filters are designed for single use to avoid cross-contamination. Reusing a filter increases the risk of clogging (from dried condensate or debris) and reduced performance, which could compromise BI accuracy.
Company Details
Business Type:
Manufacturer,Exporter,Seller
Year Established:
1994
Total Annual:
$15,000,000-$25,000,000
Employee Number:
101~135
Ecer Certification：
Verified Supplier
Founded in 1994, Zhejiang XINNA Medical Device Technology Co.,ltd is a trusted and professional manufacturer of high-quality membrane filtration products. As a high-tech enterprise integrating R&D, production and sales, Xinna provides a wide range of membrane filter products and solutions ... Founded in 1994, Zhejiang XINNA Medical Device Technology Co.,ltd is a trusted and professional manufacturer of high-quality membrane filtration products. As a high-tech enterprise integrating R&D, production and sales, Xinna provides a wide range of membrane filter products and solutions ...
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