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उत्पाद विवरण:
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| उत्पत्ति के प्लेस: | चीन |
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| ब्रांड नाम: | No |
| प्रमाणन: | ISO9001 |
| मॉडल संख्या: | XNPF052 |
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भुगतान & नौवहन नियमों:
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| न्यूनतम आदेश मात्रा: | 500 टुकड़े |
| मूल्य: | $4.5 - $7.5 per piece |
| पैकेजिंग विवरण: | 12 पीसी/पैक मानक निर्यात दफ़्ती पैकेजिंग या अनुकूलित |
| प्रसव के समय: | 35 दिन |
| भुगतान शर्तें: | एल/सी, टी/टी |
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विस्तार जानकारी |
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| प्रोडक्ट का नाम: | बैक्टीरियल एयर वेंट फ़िल्टर | आवास व्यास: | 52 मिमी |
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| निस्पंदन व्यास: | 40 मिमी | फ़िल्टर मीडिया: | पीटीएफई |
| रोम छिद्र के आकार का: | 0.22μm | वायु प्रवाह: | दिशाहीन |
| आवास सामग्री: | पीपी | रंग: | सफेद और पारदर्शी या अनुकूलित |
| आवेदन: | एयर वेंटिंग और गैस निस्पंदन | फ़िल्टर दक्षता: | 95% तक |
| ओईएम: | उपलब्ध | ||
उत्पाद विवरण
40mm 0.2 micron PTFE Hydrophobic Bactria Filter For Suction Unit Aspirator
The bacteria filter is constructed with a polytetrafluoroethylene (PTFE) membrane, offering excellent resistance to both organic and inorganic chemical corrosion, as well as inherent hydrophobicity. It is widely used in biotechnology, pharmaceutical industries, laboratories, and any process requiring sterile venting. The product is lightweight, safe, and reliable, with no risk of tube kinking that could obstruct ventilation.
Product Features:
Applications:
Specifications
Filter Media: Hydrophobic PTFE laminated with polypropylene
Filtration : 0.22μm
Housing: Polypropylene
Housing Diameter:52mm
Connectors: 6mm to 12mm stepped hard
Housing Height: 54mm
Filter media diameters:40mm
Sterilization: Autoclave at 121℃ 30min up 60 cycles
The development, production, and sales processes of this product comply with the ISO 9001 Quality Management System requirements.
Quality Assurance Guidelines
The following are routine inspection items:
Biocompatibility
The materials of this product have been tested and comply with USP <88> for VI-121 ℃ plastic biological reactivity testing.
Cleanliness
This product conforms to the definition of a "non-fiber releasing filter" as specified in 21 CFR 210.3(b)(6).
Indirect Food Additive
All constituent materials comply with the U.S. FDA 21 CFR 177-182 requirements for indirect food additives.
All constituent materials comply with EU Regulation 1935/2004/EC for materials intended to come into contact with food.
Maximum Differential Pressure
Withstands a forward differential pressure of 3.0 bar at 20°C.
Sterilization Method
After 60 cycles of moist heat sterilization (121°C, 30 minutes), the filter integrity test remains qualified.
Batch Release Criteria
Filters sampled from the manufacturing batch undergo the following tests:
Integrity Test
Each filter has passed a non-destructive integrity test correlated with bacterial challenge testing.
Bubble Point ≥ 1.1 bar in 60% IPA : 40% purified water.
अपना संदेश दर्ज करें
| Zhejiang Xinna Medical Device Technology Co., Ltd. |
| हुआंगनिकन उद्योग क्षेत्र, यूचेंग स्ट्रीट, युहुआन, ताइझोउ शहर, झेजियांग प्रांत, चीन। |
| +8613958193545-571-83082507 |
| xinna@zjxinna.com |
