Máy kiểm tra rò rỉ bao bì XHinstruments XHD-03

Cảm biến áp suất chênh lệch: ± 2kpa, sai số 0.5% F.S.

Độ phân giải chênh lệch áp suất: 0.1pa

Kiểm tra cảm biến áp suất: Lỗi ≤ ± 1% F.S.

Phạm vi áp suất thử nghiệm: -0.1～0.2MPa/-0.1～0.7MPa/-0.1～1.0MPa

Khẩu độ phát hiện tối thiểu: 2μm

Phương thức hiển thị: Màn hình cảm ứng màu cảm ứng 10 inch

Điện áp: AC100V-240V, 50/60Hz, công suất 200W

Trọng lượng: Chủ nhà: khoảng 30kg

Audit trail: ≥5 năm lưu trữ , có thể được truy vấn theo thời gian

Quản lý quyền: Đăng nhập bằng tên người dùng và mật khẩu, quyền cấp 4, đáp ứng yêu cầu FDA 21CFR PHẦN 11

Chức năng in: Máy in vi mô bên ngoài

Hồ sơ lịch sử: lưu trữ ≥5 năm

Sao lưu dữ liệu: Hỗ trợ đĩa U để xuất dữ liệu

Tín hiệu đầu ra: (4-20) mA, RS485, đầu ra cảnh báo 12V

Giao diện: Ethernet USB RS485

Product Description:

Packaging leak tester is suitable for sealing integrity testing of pharmaceutical packaging to prevent moisture, oxygen, and microorganisms from contaminating products. Medicines: bottled, bagged, boxed, ampoules, vials, cartridges, prefilled needles (PFS), (BFS), (FFS), etc.

Spray cans: plunger spray cans; bag-lined spray cans; "energy jacket" spray cans; flexible tube spray cans.

Test Standards: USP <1207>, ASTM F2338 standards and FDA standards

Product Features:

◎Comply with USP <1207>, ASTM F2338 standards and FDA standards.

◎Semi-automatic detection, suitable for small batch and multi-variety testing.

◎Non-destructive non-destructive testing, high accuracy, repeatability, sensitivity.

◎The instrument is used for vacuum pressure difference detection.

◎The leak rate can be automatically converted into defect aperture μm.

◎Database storage of test results for easy quality management.

◎Database storage of test results for easy quality management.

◎Touch-type man-machine interface, simple and quick operation: after setting/selecting the test program, only need to manually put in/take out the test sample.

 Advantage function:

◎Automatically test the flow rate and change the aperture size during the whole process.

◎Automatic leak rate calibration function.

◎Equipped with standard leaks (standard positive bottles, with third-party certification).

◎Four-level user authority management meets FDA 21CFR PART 11 requirements.

◎With audit trail function.

◎Split design, the test chamber is located above the host, and various test chambers can be provided according to different product types.

◎We also provide users with supporting services related to tightness testing, including positive bottle production, standard leak rate/annual leak verification, new sample mold customization, sample methodological parameter development and verification, etc.

◎The test cavity is customized according to customer needs to ensure that the test cavity is fully matched with the customer's product, and rapid and sensitive testing.