What is the lead time for production?

The average lead time is one month, or 1-3 months depending on the season.

Which international standards does the equipment comply with?

The equipment complies with EU GMP, US FDA cGMP, PICS, and WHO GMP standards.

What is the production capacity of the machine?

The capacity ranges from 1500 to 24,000 pieces per hour for large volume IV fluids.

Chemical & Pharmaceutical Machinery PP Bottle Filling and Sealing Machine

Name: Chemical & Pharmaceutical Machinery PP Bottle Filling and Sealing Machine
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2063632895

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$180,000.00-1,200,000.00

1 Piece

Product profile

After-sales Service

Field Installation, Commissioning and Training

Automation

Condition

New

Model NO.

Customized IVEN -1

Production Continuity

Continuous

Production Scope

Product Line

Function

Air Washing, Water Washing, Filling, Cap

Filling Speed

4000bph-30000bph

Key Selling Points

Energy Saving

Applicable Industries

Manufacturing Plant, Pharma

Filling Material

Water, Medical Liquid

Voltage

220V/, 50Hz/60Hz

Packaging Type

Bottles, Bags

Machine Type

Washing Filling Sealing Machine

Application

Machinery & Hardware, Medical

Core Components

Motor, PLC

Machinery Capacity

Customized

Warranty

1 Year

Transmission Type

Flexible

Automatic Production Line

Comprehensive

Flexible Production

Intelligent Manufacturing

Transport Package

Wooden Case

Specification

9620.00cm * 2540.00cm * 2330.00cm

Trademark

IVEN

Origin

China

Production Capacity

Customized

Key features

Turnkey Project Expertise: Leader in IV solution turnkey projects with over 19 years of global experience.

Global Compliance Standards: Compliant with EU GMP, US FDA cGMP, PICS, and WHO GMP standards.

Flexible Customization: Offers full, minor, and flexible customization from samples or designs.

Comprehensive After-Sales: Includes field installation, commissioning, training, and spare parts for n years.

High Production Capacity: Capable of producing 1500 to 24,000 pieces per hour for large volume IV fluids.

Proven International Track Record: Successfully delivered projects to over 40 countries across multiple continents.

Energy Saving Design: Key selling point focused on energy efficiency for sustainable manufacturing.

100% Quality Inspection: Strict visual and function inspection for all finished products before shipment.

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: ≤2.27h 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.