Medshine
Medshine
Medshine M126 Semi-Automatic Sperm An...
Medshine M126 Semi-Automatic Sperm Analyzer
The Medshine M126 Semi-Automatic Sperm Analyzer is an intelligent semen-analysis system for modern reproductive medicine. It combines computer image processing with artificial intelligence technology for sperm identification, sperm-motion tracking and quantitative analysis of sperm dynamic and static characteristics.
Key Features
- WHO 5th software referenced by the manufacturer source page.
- Simple guided operation for routine laboratory users.
- Automatic sperm identification and motion tracking with trajectory display.
- Analyses more than 30 sperm parameters including density, motility, movement trajectory, movement map and total sperm count.
- Supports morphology analysis, TZI and SDI calculations, report customization, playback/audit functions and LIS/HIS/network sharing depending on configuration.
Specification Highlights
- Model: M126; brand: Medshine.
- Maximum tested sperm count: 1000.
- Test speed range: 0 to 180 um/s.
- Frame number of picture: 0 to 75.
- Particle diameter resolution: 0 to 150 um/s as listed by the source page.
- Analysis time: 1 to 5 seconds or longer.
- Collected image groups: 1 to 25 groups.
- Microscope objective lens options listed: 10x, 20x, 40x and 100x.
- Standard configuration listed: main unit, all-in-one PC, microscope, camera and English analyzer software.
- Certificate/warranty shown by source: CE, ISO; 18 months.
Clinical and Laboratory Applications
- Clinical semen testing and male fertility assessment support.
- Hospital laboratories, fertility clinics, andrology laboratories and reproductive medicine centres.
- Laboratories requiring sperm motility, morphology and semen-analysis reporting functions.
Procurement and Configuration Notes
- Please confirm final microscope type, camera, software version, PC specification, language, consumables and LIS/HIS integration before ordering.
- The source page lists CE and ISO, but certificate copies and market-specific regulatory status should be verified before procurement.
- Clinical use should be supported by validated SOPs and trained laboratory personnel.
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