What certifications does the machine have?

The machine is certified with CE, GMP, and ISO standards.

What is the power supply requirement?

The machine requires a 3-phase 380V 50Hz power source, with power consumption ranging from 8KW to 60KW depending on the model.

Customized Intravenous Fluid Manufacturing Normal Saline Fluids Production IV Drip Machine with GMP Good Service

Name: Customized Intravenous Fluid Manufacturing Normal Saline Fluids Production IV Drip Machine with GMP Good Service
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2072276985

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$200,000.00-350,000.00

1 Piece

Product profile

Application

Machinery & Hardware, Medical&Pharmaceutical;

Disposable

Injection Site

Intravenous

Model NO.

CUSTOMIZED 1

Usage

Chemical, Medical, Food

Warranty

1 Year

Feature

Durable, Quick Changeover;

Filling Volume

20--1000ml(Customized)

Capacity

Customized

Machine Weight

2000-3000kg

Certificate

CE, ISO, SGS

Driven Type

Electric

Machine Size

3000*2000*1800mm

Power

380V 50Hz

Used for

Chemical, Medical, Food, Pharmaceutical

Function

Washing, Filling, Capping, Labelingsealing, Packing

Bag-Making Film

Non-PVC Film

Key Selling Points

Automatic;Energetic;Easy to Operate;

Bag-Making Form

Single Port, Heat Insulation Seal

Finished Dosage Form

Liquid

Precision

High Precision

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Customized

Condition

New, 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

High Precision Filling: Uses E+H mass flowmeter for accurate filling with no overflow or particle generation.

100% Film Utilization: No waste edge between bags, reducing material and energy consumption significantly.

Quick Changeover: Switch from one size to another in just 0.5-1 hour by changing mould and printing panel.

Low Leakage Rate: Reliable heating and welding system ensures leakage rate is less than 0.03%.

Compact Structure: Reduces machine length by 1/3, saving room space and running costs.

Smart Control System: PLC with multi-language touch screen, auto detection, and strong memory for parameters.

Versatile Application: Suitable for 50-5000ml Non-PVC soft bags for solutions, antibiotics, and dialysis fluids.

GMP Certified: Machine meets CE, GMP, and ISO standards for pharmaceutical production safety.

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.