

LED Fluorescence Microscope for Clinical Diagnostics
临床诊断 LED 荧光显微镜
- SKU CLM-0003
- Clinical Microscopy
- CE (to be confirmed)
- ISO 13485 quality system (to be confirmed)
Price on request — FOB / CIF quoted per order
Prices depend on configuration, quantity and destination port.
Key specifications
| Observation method | Epifluorescence and brightfield |
|---|---|
| Excitation source | LED, 450–470 nm (blue), optional UV/green |
| Filter cubes | 2–4 positions |
| Objectives | Fluor 10×/20×/40×/100× oil |
| Magnification | 100×–1,000× |
| LED lifetime | > 10,000 h |
By Lab Manufacturers China Technical TeamLast reviewed Standards: ISO 8039, ISO 10110, IEC 61010-1
What is the LED Fluorescence Microscope for Clinical Diagnostics?
An LED fluorescence microscope excites fluorescent dyes or labeled antibodies with LED light and images them through barrier filters. It is used for auramine-stained tuberculosis smears, immunofluorescence of autoantibodies and malaria or parasite screening in clinical laboratories.
What is the LED Fluorescence Microscope for Clinical Diagnostics?
An LED fluorescence microscope excites fluorescent dyes or labeled antibodies with LED light and images them through barrier filters. It is used for auramine-stained tuberculosis smears, immunofluorescence of autoantibodies and malaria or parasite screening in clinical laboratories.
Overview
This variant adds an epifluorescence illuminator to a brightfield stand. A high-power LED at about 450 to 470 nm excites fluorophores such as auramine O, FITC and acridine orange, and an excitation filter, dichroic mirror and emission filter pass only the emitted light to the eyepiece. Filter cubes for blue, green and UV are swappable. Compared with mercury lamps, LEDs switch on instantly, consume less than 20 W, last more than 10,000 hours and require no lamp alignment, which reduces running cost and ozone exposure. Fluorescence objectives include 10×, 20×, 40× and 100× oil with high numerical aperture and low autofluorescence. Auramine smears can be screened at 20× or 40×, which is faster than 100× Ziehl-Neelsen screening. Some models combine brightfield and fluorescence in one unit.
How does it work?
A compound microscope forms an enlarged image in two stages. The objective lens creates a real intermediate image of the specimen, and the eyepiece magnifies it further, giving total magnification equal to objective power times eyepiece power, commonly 40× to 1,000×. A condenser focuses light from an LED or halogen source onto the specimen using Köhler illumination for even contrast. Phase-contrast optics convert small refractive index differences in live cells into intensity differences using a phase ring. Dark-field blocks direct light so only scattered light enters the objective, making thin organisms bright on dark background. Fluorescence microscopes use an excitation filter, dichroic mirror and emission filter to show fluorophore-labeled targets. Digital systems add a camera or scanner that captures images and stitches fields into whole slide images.
What are the key features?
- High-power LED excitation at about 450–470 nm
- Swappable filter cubes for blue, green and UV excitation
- Fluorescence objectives 10× to 100× with low autofluorescence
- Instant on and off with lifetime over 10,000 hours
- No lamp alignment and lower power than mercury lamps
- Combined brightfield and fluorescence operation
What are the technical specifications?
A typical led fluorescence microscope for clinical diagnostics configuration offers observation method of Epifluorescence and brightfield, excitation source of LED, 450–470 nm (blue), optional UV/green, filter cubes of 2–4 positions, objectives of Fluor 10×/20×/40×/100× oil, magnification of 100×–1,000× and LED lifetime of > 10,000 h. Values are indicative of the product class; the exact figures for each configuration are confirmed on the quotation and the calibration documents supplied with the instrument.
Which applications is it used for?
The LED Fluorescence Microscope for Clinical Diagnostics is used in auramine-stained tuberculosis smear screening, autoantibody immunofluorescence, malaria and parasite screening and fungal fluorescent staining. Across the wider Clinical Microscopy class, laboratories also deploy it for blood film differential examination, urine sediment examination and microbiology smear examination.
Which standards and certifications apply?
Relevant standards and methods include ISO 8039, ISO 10110, IEC 61010-1, ISO 15189, ISO 19012-1 and ISO 19012-2. Certification candidates for this model are CE and ISO 13485 quality system; each is to be confirmed for the specific configuration before shipment, and certificates are supplied only where they have been issued.
Place the microscope on a stable, vibration-free bench away from direct sunlight and dust, and use a cover when idle. Clean lenses only with lens tissue and approved solvent, and remove immersion oil after each use. Align Köhler illumination and verify parfocality at installation and after servicing. Calibrate eyepiece reticles or camera scale with a stage micrometer for measurements. Replace LED or halogen sources according to lifetime, and inspect objectives for scratches and fungus in humid climates. Staff should observe ergonomic posture and breaks. For digital systems, validate image quality and storage integrity in line with laboratory procedures under ISO 15189.
How do I select the right LED Fluorescence Microscope for Clinical Diagnostics?
Select this variant for acid-fast fluorescent screening, immunofluorescence and other fluorophore-based tests. In the RFQ specify the excitation wavelengths and filter cubes required, objective types and numerical apertures, LED lifetime, camera port and whether combined brightfield operation is needed. Ask for sample images of reference slides.
How does it compare with other Clinical Microscopy variants?
Choose the microscope by specimen type and contrast technique. Brightfield with plan achromat objectives suits stained blood films, Gram stains and histology. Phase contrast is preferred for unstained urine sediment, semen and live cell culture. Dark-field suits spirochetes such as Treponema pallidum, and fluorescence suits auramine acid-fast screening and immunofluorescence. Check objective quality, numerical aperture, field number, stage mechanics, illumination life and whether a camera port or digital system is needed for documentation and telepathology. Consider ergonomic features such as tilting binocular heads and low stage height for long screening sessions, and confirm objective parfocality and availability of spare lamps and service support.
Full specifications
| Observation method | Epifluorescence and brightfield |
|---|---|
| Excitation source | LED, 450–470 nm (blue), optional UV/green |
| Filter cubes | 2–4 positions |
| Objectives | Fluor 10×/20×/40×/100× oil |
| Magnification | 100×–1,000× |
| LED lifetime | > 10,000 h |
| Power consumption | < 20 W (fluorescence unit) |
| Head | Binocular or trinocular |
| Camera port | Optional C-mount |
| Stage travel | 75 × 50 mm |
| Power supply | 100–240 V AC, 50/60 Hz |
Indicative values for this product class. Final specifications are confirmed on the quotation and in the calibration documents supplied with the instrument.
Applications
- Auramine-stained tuberculosis smear screening
- Autoantibody immunofluorescence
- Malaria and parasite screening
- Fungal fluorescent staining
Key features
- High-power LED excitation at about 450–470 nm
- Swappable filter cubes for blue, green and UV excitation
- Fluorescence objectives 10× to 100× with low autofluorescence
- Instant on and off with lifetime over 10,000 hours
- No lamp alignment and lower power than mercury lamps
- Combined brightfield and fluorescence operation
Frequently asked questions about LED Fluorescence Microscope for Clinical Diagnostics
It is used to detect fluorescent-stained or labeled targets, for example auramine-stained Mycobacterium tuberculosis, autoantibody patterns on tissue substrates, parasites stained with acridine orange and fungal elements with calcofluor white. Fluorescence gives high contrast even with very few organisms.
LED sources switch on instantly, last more than 10,000 hours versus about 200 hours for a mercury lamp, use less power and need no alignment or warm-up. They also avoid mercury disposal and ozone, making them safer and cheaper to run in routine laboratories.
Photobleaching is reduced by minimizing exposure time, lowering LED intensity, using neutral density filters, and examining slides promptly after staining. Antifade mounting media help for immunofluorescence, and slides are stored in the dark at 2 to 8 °C.
It is used to examine specimens under magnification for diagnosis, including blood cell morphology, urine sediment, parasites, bacteria in stained smears, cytology and tissue sections. Different microscope types provide brightfield, phase-contrast, dark-field or fluorescence contrast for different specimens.
Standard objectives are 4×, 10×, 40× and 100× oil immersion, paired with 10× eyepieces to give 40× to 1,000× total magnification. Low power locates fields, 40× is used for urine sediment and cytology, and 100× oil is used for blood films and bacterial morphology.
Köhler illumination is a method of adjusting the field and condenser apertures so the specimen is evenly lit and glare is minimized. It gives maximum resolution and contrast from the objective, and should be set after installing or moving the microscope and when changing objectives.





