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Thông tin chi tiết sản phẩm:
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| Nguồn gốc: | Trung Quốc |
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| Hàng hiệu: | No |
| Chứng nhận: | ISO9001 |
| Số mô hình: | XNPF052 |
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Thanh toán:
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| Số lượng đặt hàng tối thiểu: | 500 mảnh |
| Giá bán: | $4.5 - $7.5 per piece |
| chi tiết đóng gói: | 12 cái/gói bao bì carton tiêu chuẩn xuất khẩu hoặc tùy chỉnh |
| Thời gian giao hàng: | 35 ngày |
| Điều khoản thanh toán: | L/C, T/T. |
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Thông tin chi tiết |
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| Tên sản phẩm: | Bộ lọc lỗ thông hơi vi khuẩn | đường kính nhà ở: | 52mm |
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| Đường kính lọc: | 40mm | Bộ lọc phương tiện: | PTFE |
| Kích thước lỗ chân lông: | 0,22μm | Luồng không khí: | một chiều |
| Vật liệu nhà ở: | Pp | Màu sắc: | Trắng và trong suốt hoặc tùy chỉnh |
| Ứng dụng: | Thông gió và lọc khí | Hiệu quả lọc: | Lên đến 95% |
| OEM: | có sẵn | ||
Mô tả sản phẩm
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.
Nhập tin nhắn của bạn
| Zhejiang Xinna Medical Device Technology Co., Ltd. |
| Khu công nghiệp Huangnikan, đường Yucheng, Yuhuan, thành phố Taizhou, tỉnh Zhejiang, Trung Quốc. |
| +8613958193545-571-83082507 |
| xinna@zjxinna.com |
