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GMP-Compliant Form-Fill-Seal Machines for IV Solutions/ IV Fluids
US$150,000.00-1,200,000.00
1 Piece

Product profile

Application

Machinery & Hardware, Medical&Pharmaceutical;

Warranty

1 Year

Feature

Durable, Quick Changeover;

Model NO.

customized

Filling Volume

20--1000ml

Capacity

Customized

Type

Pharmaceutical Packaging Machinery

Finished Dosage Form

Liquid

Precision

High Precision

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Computerized

Customized

Customized

Condition

New

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

GMP Compliant Design: Fully compliant with GMP standards for IV solutions and pharmaceutical packaging.
One-Line Multi-Bag Production: Produces two different bag types with single or double ports on one line.
High Precision Filling: Uses E+H mass flowmeter for accurate filling with no qualified bag waste.
Customized Capacity: Filling volume customizable from 20ml to 1000ml with quick mold changes.
Low Leakage Rate: Advanced heat sealing technology ensures leakage rate below 0.3 per mille.
Multi-Language Touch Screen: Interface supports Chinese, English, Spanish, Russian and other languages.
Compact Structure: Space-saving design with smaller footprint for efficient factory layout.
1-Year Warranty: Comprehensive 1-year warranty coverage for all mechanical equipment.

Company profile

Shanghai Iven Pharmatech Engineering Co., Ltd.
Years of Export ExperienceLow MOQPatents AwardedProduct Certification
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: ≤2.46h 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.

Product Q&A

Q:What is the filling capacity range?
A:
The machine supports filling volumes from 20ml to 1000ml, with specific specifications available in 100, 250, 500, and 1000ml.
Q:Can the machine produce different bag types?
A:
Yes, one production line can make two different types of bags with single or double hard ports.
Q:What is the production capacity?
A:
Production capacity ranges from 900 to 8000 bottles per hour (bph) depending on the model and bag size.
Q:Is the machine GMP compliant?
A:
Yes, the machine is designed to be GMP compliant and is suitable for IV solutions, dialysis, and parenteral nutrition.
Q:What is the warranty period?
A:
We provide a 1-year warranty for the machine.

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