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Product profile
Customization
AvailableClassification
Hearing Diagnostic EquipmentType
Middle Ear Analyzer TympanometerModel NO.
MD-6510Certification
CE, FDA, MSDS, ISO13485Group
AllKey features
Comprehensive Middle-Ear Testing-Diagnostic & screening tympanometry
ETF Testing-For intact and perforated eardrums
Advanced Acoustic Reflex Testing-Threshold, decay & latency; IPSI & CONTRA
Automatic Screening-Fast tympanometry, reflex & decay screening
Accurate Impedance Measurement-Reliable middle-ear function assessment
Stable Air Pressure System-Precise and consistent testing
Flexible Stimuli-Supports various clinical testing requirements
Company profile

Business Type: Manufacturer/FactoryExport Year: 2004-01-09Nearest Port: TIANJINAverage Response Time: ≤18hTerms of Payment: T/T, Western UnionInternational Commercial Terms(Incoterms): FOB, CIF, EXW
AI-Powered supplier vetting
SummaryMEDA Co., Ltd. is identified as a China-based manufacturer/factory of ophthalmic medical equipment, with a Tianjin location and state-owned ownership. The supplier reports ISO 13485 certification, more than 10 production lines, an AB Scanner annual productivity figure of 500 pieces, and peak-season fulfillment within one month. Its product scope includes ophthalmic scanners, biometers, pachymeters, lasers, and related devices. R&D resources are supported by 31–40 years of combined engineer experience, while 6–10 quality-control staff are reported. The evidence supports production capability, medical-device specialization, and innovation resources. After-sales service, customization, and specific customer cases are not sufficiently documented. Financial credibility cannot be fully assessed from the available non-financial information.
Supplier typeThe supplier is explicitly classified as a Manufacturer/Factory and operates in health and medicine. Its stated product scope centers on ophthalmic ultrasonic and related medical equipment, indicating direct manufacturing specialization rather than only trading or distribution.
CertificationsMEDA reports holding ISO 13485 certification, a medical-device quality management system certification. This is explicit evidence of a relevant management-system qualification.
R&D capabilityThe supplier reports 31–40 years of total R&D-engineer experience, origins linked to the Institute of Biomedical Engineering of the Chinese Academy of Medical Sciences, and continued development of new products. These details explicitly support substantial technical and product-development capability.
Production capacityMEDA reports more than 10 production lines, AB Scanner productivity of 500 pieces, 6–10 quality-control staff, and order fulfillment within one month during peak season. These stated operating indicators support meaningful manufacturing capacity, although the productivity figure is specific to the AB Scanner and should not be generalized to all products.
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