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The Perlong Medical Equipment BTX-9800 is a 3.6 kW mammography X-ray system engineered for breast cancer screening and diagnostic imaging, featuring a rotating anode X-ray tube and high-frequency inverter technology that delivers stable kV output for consistent image quality. The unit produces high-resolution mammographic images with optimised contrast for dense breast tissue visualisation, supported by a dedicated image acquisition workstation. The 3.6 kW power rating positions it as a mid-capacity system suitable for medium-patient-volume facilities requiring reliable screening throughput without the capital outlay of premium 5-8 kW systems.
The system architecture employs a motorised C-arm with vertical升降运动 (typical range 550-850 mm for patient table height adjustment) and an integrated compression device with force feedback, typically adjustable from 70-180 N to standardise breast compression across varying tissue densities while maintaining patient comfort parameters. The image receptor is a direct digital detector, standard for current-generation mammography, eliminating film processing and enabling immediate image review. Typical detector formats for this class of equipment are 18 x 24 cm and 24 x 30 cm, accommodating standard cranio-caudal and medio-lateral oblique projections. The control interface utilises a touchscreen panel with preset anatomical programmes (APR) for routine screening and diagnostic views, with manual override capability for custom exposure parameters.
Target buyers include hospital radiology departments, dedicated breast imaging centres, and outpatient diagnostic clinics in developing healthcare markets seeking CE-compliant equipment at competitive capital cost points. The BTX-9800 is suited for facilities performing 10-30 mammography procedures daily, with digital image storage compatible with PACS integration via DICOM 3.0 protocol (standard for this equipment class). Buyers should confirm with Perlong Medical Equipment whether the supplied configuration includes the acquisition workstation, DICOM connectivity licence, and compression paddle set as standard or optional items. Shipping terms and installation support from the Nanjing facility require direct negotiation, as the listing does not specify Incoterms, lead times, or post-installation calibration protocols.
| Generator Power Output | 3.6 kW (typical for single-phase mid-capacity mammography systems) |
| X-Ray Tube Type | Rotating anode, molybdenum or rhodium target (standard for dedicated mammography) |
| kV Range | 20-35 kV (typical mammography operating range for optimal soft-tissue contrast) |
| mA Range | 10-120 mA, with automatic exposure control (AEC) standard for this class |
| Anode Heat Storage | 300-400 kHU typical for 3.6 kW systems; confirm exact HU rating with supplier |
| Image Receptor | Direct digital flat-panel detector (a-Si or a-Se technology, standard specification) |
| Detector Active Area | 18 x 24 cm and/or 24 x 30 cm (standard mammography formats; confirm included sizes) |
| Compression Force | Adjustable 70-180 N with force display, typical for digital mammography systems |
| Patient Table Vertical Travel | Approximately 550-850 mm (typical range; confirm exact travel with supplier) |
| Image Output Protocol | DICOM 3.0 for PACS integration (standard; confirm software licence inclusion) |
Perlong Medical Equipment Co., Ltd. maintains its registered address at No.168 Kaiyuan Road, Jiangning District Science Park, Nanjing 211112, Jiangsu Province, China, placing its manufacturing and administrative operations within the Nanjing Jiangning economic and technological development zone. The supplier is classified at imported tier with harbour trust designation, indicating that its profile has undergone a verification process within the marketplace framework. The response rate is recorded at 0.00 with zero average response hours, which buyers should interpret cautiously: this may reflect a newly listed profile, a temporary data synchronisation gap, or limited active engagement on this platform channel. Direct contact through the provided Jiangnan address or a verified trade communication channel is advisable to assess real-time responsiveness.
The listing presents the BTX-9800 mammography system as the core product, positioning Perlong as a manufacturer or authorised distributor of diagnostic imaging equipment for breast cancer screening. No employee count, annual revenue, factory certification specifics, or client reference installations are stated in the available profile data. The company does not disclose ISO 13485 medical device quality management certification, CE marking documentation references, or FDA registration status in the extracted facts. Buyers should request copies of the Medical Device Registration Certificate for China (NMPA), EU Declaration of Conformity for CE marking, and ISO 13485 certificate directly from Perlong Medical Equipment before advancing to purchase negotiation. The absence of stated MOQ, price bands, or lead times in the source material means these commercial terms require explicit confirmation.
| Business Type | Supplier |
| Year Established | Recently Joined |
| Employees | Contact Supplier |
| Annual Revenue | Contact Supplier |
| Main Products | View Products Tab |
| Major Markets | Global |
| Response Time | <4h |
| Response Rate | New Supplier |
Before placing an order for the BTX-9800, verify that Perlong Medical Equipment holds valid NMPA registration for Class III medical device manufacture in China, and request copies of the EU Declaration of Conformity if CE marking is claimed. Confirm that the detector, generator, and workstation are from single-source manufacture or validated subsystem integration, as mixed-component systems may complicate regulatory clearance in your destination country. Ask for reference installations with contactable end users, and verify that software language localisation, operator training materials, and technical documentation are available in your required language. The 0.00 response rate in the profile data necessitates proactive direct outreach to validate supplier engagement before deposit payment.
Logistics from Nanjing Jiangning Science Park typically route through Shanghai Port or Nanjing Lukou Airport for international shipment. Confirm with Perlong whether standard Incoterms are EXW, FOB Shanghai, or CIF destination port, and whether export crating meets ISPM-15 phytosanitary standards for wooden packaging. Medical equipment requires careful handling; verify if Perlong uses specialised medical device freight forwarders familiar with shock-sensitive cargo. Lead times for mammography systems commonly range 6-12 weeks from order confirmation, but this estimate requires direct confirmation. Payment terms should be structured with milestone-based release: 30% deposit, 60% against shipping documents, and 10% post-installation acceptance, with a confirmed irrevocable letter of credit for initial transactions given the response rate uncertainty.
Quality assurance at receipt should include detector uniformity testing using a homogeneous phantom, kV accuracy verification with a calibrated dosimeter, and compression force calibration against a certified load cell. Engage an independent biomedical engineering inspector or your country's authorised representative for pre-shipment factory acceptance testing (FAT) at the Nanjing facility if travel budgets permit. Documentation to demand includes: NMPA registration certificate, ISO 13485 certificate, CE technical file summary, electrical safety test report per IEC 60601-1, and electromagnetic compatibility (EMC) test results. Post-installation, require Perlong to perform beam quality verification, AEC reproducibility testing, and radiation dose output measurement against diagnostic reference levels before final acceptance.
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