Biobase Elisa Processor Open System Fully Automatic Elisa Processor for Hospital

Name: Biobase Elisa Processor Open System Fully Automatic Elisa Processor for Hospital
Brand: Biobase Biodustry (Shandong) Co., Ltd.
SKU: 743298712

Shandong, ChinaBiobase Biodustry (Shandong) Co., Ltd.

US$9,000.00-9,400.00

1 Piece

Product profile

Customization

Available

Classification

Biochemical Apparatus

Type

Biochemistry Analyzer

Model NO.

BIOBASE1000

Certification

CE, FDA, ISO13485

Group

All Ages

Product Name

Auto Elisa Processor

Sample Racks

Standard 192 Sample Position (Expandable, up to 38

Pipetting

10~1000μL

Dispensing System

1 Aspirating-Dispensing Probe with X-Y-Z Movement;

Reagent Racks

Universal Reagent Position: Standard 6 Universal R

Pipetting Range

10~1000μL,1μL Stepping

Pipetting Precision

(100μL) CV≤0.5%

Dispensingtime

5 Minutesto Whole96well Microplates

Incubation

2 Independent Incubators

Temperature Range

Rt to 45 °C

Temperature Accuracy

±0.5°C

Washing Probes

Two Line 8-Nozzle Manifolds

Wash Containers

2 Wash Buffers 2L, 1 Distilled Water, 1 Waste Wate

Washing Residual

<2μL

Reading Channels

8 Independent Photometric Channels,

Transport Package

Wooden Package

Specification

1085*840*1318mm

Trademark

BIOBASE

Origin

China

Production Capacity

1000PCS/Month

Company profile

Importers and ExportersYears of Export ExperienceExperienced TeamExhibition Experience

Biobase Biodustry (Shandong) Co., Ltd.

Shandong, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 15 years CertifiedNearest Port: Qingdao PortAverage Response Time: ≤3.73h

AI-Powered supplier vetting

SummaryThe supplier is identified as a combined company involved in medical-device sales, manufacturing, research and development, and related technical activities. It reports ISO9001:2015, ISO14001, and CE certifications, 100% finished-product inspection, five quality inspectors, and stated annual production capacities for Biological Safety Cabinets and Auto Chemistry Analyzers. R&D evidence includes new products in the past year, ODM services, and broad customization from samples, designs, or full specifications. Overseas support includes installation, repair, training, maintenance, and debugging, with overseas warehouses and agents or branches. Financial records are identified for 2022–2024, but no financial performance values are provided. Evidence of customer cases is limited to OEM service for popular brands and participation in the Pittcon Exhibition.

Supplier typeThe supplier is classified as a combined company. Its stated scope covers Class I, II, and III medical-device activities, including sales, production, research and development, medical services, and related installation or construction activities.

CertificationsThe supplier reports ISO9001:2015 and ISO14001 certifications, as well as CE product certification capability. The slices do not provide certificate validity dates or scope details, but they explicitly identify multiple certifications.

After-Sales capabilityThe supplier lists overseas installation, repair, training, maintenance, and debugging services, and reports overseas warehouses plus overseas agents or branches. It also has written service-capability procedures with follow-up records and 20 qualified service suppliers, although the stated overseas-service country count is zero.

R&D capabilityThe supplier reports new products during the past year, provides ODM services, and offers broad R&D customization. It does not have an available SDK, which limits evidence of software-development support but does not negate the documented product-development capability.

Production capacityThe supplier reports annual capacities of 10,000 Biological Safety Cabinets and 11,100 Auto Chemistry Analyzers, with laser cutting equipment and a bending machine. Its stated business scope also includes production of Class I, II, and III medical devices, while the adequacy of equipment and capacity for a specific order is not established.

Customization capabilityBoth R&D and design-capability records list customization from samples, customization from designs, full customization, minor customization, and flexible customization. This is explicit evidence of a broad customization offering.