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CE Approved Medical 3 Part Diff Hematology Analyzer (WHY6390)
US$1,500.00-3,000.00
1 Piece
Product profile
Customization
AvailableClassification
Biological DiagnosticsType
Urine AnalyzerModel NO.
WHY6390Certification
CE, ISO13485Group
Neonatal, Child and AdultCalibration
Manual and Automatic CalibrationAperture
Wbc 80um Rbc/Plt 50umPower Supply
AC220V-230V/50Hz or AC110V-120V/50-60HzResults Storage
Storage of 10, 000 Patients' ResultsStandard Working Model
Dual-Channel TestingSample Pre-Dilution
Internal Diluter, Add 1 Ml Diluent AutomaticallyDisplay
10.4 " Color LCDTransport Package
Wooden PalletSpecification
ISO, CE, FDA, FSCTrademark
PoweamOrigin
ChinaHS Code
90278099Production Capacity
800PCS/MonthCompany profile

Business Type: Manufacturer/FactoryExport Year: 2003-03-01Nearest Port: shanghai,ningboAverage Response Time: ≤24hTerms of Payment: LC, T/T, D/P, etc.International Commercial Terms(Incoterms): FOB, EXW, CFR, CIF, CIP, CPT, Others
AI-Powered supplier vetting
SummaryNanjing Poweam Medical Co., Ltd. is identified as a China-based manufacturer/factory in Nanjing, Jiangsu, focused on medical equipment including ultrasound, X-ray, ECG, IVD, microscope, and related products. The supplier reports ISO 9000, ISO 13485, and ISO 9001 certifications, more than 10 production lines, 50 R&D engineers, 50 quality-control staff, and stated technical support, training, installation backup, and registration assistance. It has exported since 2003 and serves multiple global regions, with stated order fulfillment within 15 working days in both peak and off-peak periods. However, the available trade records show only one transaction for each of two closely related microscope listings, so customer-case depth is limited. No sufficient evidence is provided to assess financial credibility, product customization, or measurable innovation output.
Supplier typeThe supplier is explicitly identified as a Manufacturer/Factory and a wholly foreign-owned enterprise located in Nanjing, China. Its stated business covers health and medicine and a broad range of medical equipment, supporting classification as a medical-device manufacturer rather than only a trading company.
CertificationsThe supplier reports holding ISO 9000, ISO 13485, and ISO 9001 management-system certifications. ISO 13485 is specifically relevant to medical-device quality management, providing explicit positive evidence for this field.
After-Sales capabilityThe supplier states that it provides on-the-ground launch assistance, product advice, equipment and installation training, technical-engineer support, backup, registration facilitation, and relevant certificates when necessary. Its export experience since 2003 and stated global market coverage further support service experience, although no service-response metrics are provided.
Production capacityThe supplier reports more than 10 production lines, 50 quality-control staff, and stated fulfillment within 15 working days in both peak and off-peak seasons. These explicit capacity and delivery statements support a positive assessment, although actual capacity by product category is not specified.
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