What is the minimum order quantity?

The Minimum Order Quantity is 1 Set.

What are the payment terms?

Accepted payment terms include LC, T/T, D/P, PayPal, Western Union, and Small-amount payment.

What is the lead time for production?

Lead time is one month during peak season and 1-3 months during off-season.

Normal Saline Intraveous Fuids Production Machine with CE and ISO

Name: Normal Saline Intraveous Fuids Production Machine with CE and ISO
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2070316665

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$250,000.00-1,200,000.00

1 Piece

Product profile

Application

Machinery & Hardware, Medical&Pharmaceutical;

Capacity

Customized

Certification

CE, GMP, ISO, CE

Model NO.

Customized IVEN -1

Feature

Durable, Quick Changeover;

Filling Volume

20--1000ml

Type

Pharmaceutical Packaging Machinery

Finished Dosage Form

Liquid

Precision

High Precision

Voltage

380V

Computerized

Customized

Condition

New

Warranty

1 Year

After-sales Service

Field Maintenance and Online Video Support

Transport Package

Wooden Case, Cartons

Specification

3.26x2.0 x2.1M

Trademark

IVEN

Origin

China

Production Capacity

20 PCS/Year

Key features

Non-PVC Soft Bag Production: Advanced line for automatic film feeding, printing, bag making, filling, and sealing.

High Precision Filling: Uses E+H mass flowmeter and high-pressure system for accurate filling with no qualified bag waste.

Flexible Customization: Capacity and bag designs (single/double ports) are customizable to meet specific client needs.

Intelligent PLC Control: Features touch screen with multi-language support, data adjustment, and automatic fault display.

Dual Bag Type Capability: One production line can manufacture two different types of bags with single or double hard ports.

CIP and SIP System: Special cleaning and sterilization processes save time and ensure high hygiene standards.

CE and ISO Certified: Machine meets international safety and quality standards with CE and ISO certifications.

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: ≤2.29h 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.