What is the lead time for production?

The lead time is one month during the off-season and 1-3 months during the peak season.

Biologic Drug Formulation Mixing Tank

Name: CE Approved Vaccine Blending Vessel /Vaccination Solution Mixer /Biologic Drug Formulation Mixing Tank
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 1929787451

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-350,000.00

1 Piece

Product profile

After-sales Service

Field Installation, Commissioning and Training

Application

Liquid with Suspended Solids, Powder, Viscous Fluid, Liquid, Granules, 1 Year

Application Area

Pharmaceutical

Model NO.

Customized IVEN -3

Certification

CE, ISO, CE

Condition

New

Heating Method

Electric Heating/Steam Heating

Stirring Type

Gravity

Warranty

1 year

Working

High Speed Mixer

Key Selling Points

Long Service Life;Automatic;Competitive Price

Video Outgoing-Inspection

Provided

Core Components

Motor, Pressure Vessel

Function

Mixed Dispersive Emulsification Homogene

Type

Horizonal/Vertical

Max. Loading Volume (L)

50000 L

Barrel Volume (L)

50L-50000L

Applicable Industries

Manufacturing Plant

Capacity

Customized

Layout Type

Horizontal

Operating type

Continuous Operating

Transport Package

Export Standard Package

Specification

customized

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

High-Quality Stainless Steel: Constructed with SUS316L/SUS304 stainless steel for durability and hygiene.

Customizable Capacity: Available in volumes from 50L to 50,000L to meet specific production needs.

Hygienic Design: Smooth interior surface and dead-angle-free bottom valve prevent bacterial growth.

Efficient Mixing System: Low shear mixing paddle with stepless speed regulation up to 350rpm.

CE & ISO Certified: Meets strict regulatory requirements for safety and quality standards.

Online Steam Sterilization: Supports online sterilization to ensure a sterile environment for vaccines.

Comprehensive After-Sales: Includes field installation, commissioning, and training services.

Company profile

Years of Export ExperienceLow MOQPatents AwardedProduct Certification

Shanghai Iven Pharmatech Engineering Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤1.47h CertifiedTerms of Payment: LC, T/T, D/P, etc.

AI-Powered supplier vetting

SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.

CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.

After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.

R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.

Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.

Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.