Is the equipment compliant with international standards?

Yes, we design and manufacture equipment according to GMP, FDA, WHO, ISO, and CE requirements.

What is the lead time for production?

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

Can you arrange a visit to your user sites?

Yes, we can invite you to visit our turnkey projects in countries like Indonesia, Vietnam, and Tanzania.

Automatic Sugar Syrup Making Machine/Syrup Packaging Equipment in China

Name: Automatic Sugar Syrup Making Machine/Syrup Packaging Equipment in China
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2186022925

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$30,000.00-140,000.00

1 Piece

Product profile

After-sales Service

Field Installation, Commissioning and Training

Warranty

1 Year

Type

Piston Filling Machine

Model NO.

customized

Automatic Grade

Automatic

Material Type

Liquid

Filling Valve Head

Multi-Head

Feed Cylinder Structure

Multi-Room Feeding

Dosing Device

Capacity Cup

Filling Principle

Atmospheric Pressure

Packaging Container Lifting Structure

Pneumatic Lifting

Structure

Rotary

Packaging

Bottle

Packaging Material

Plastic

Suitable for

Water or Fluid Material (Alll Liquid Washing Produ

Voltage

220V/380V, 380V 50Hz

Capacity

6000~18000 PCS/H

Applicable Syringe Specifications

5-25ml

Transport Package

Composite Materials

Specification

9000*2000*2100 mm

Trademark

IVEN

Origin

China

HS Code

8422303090

Production Capacity

Customized

Key features

Integrated Washing Filling Capping: One machine integrates washing, filling, and capping to reduce investment and production costs.

Customizable Capacity: Capacity can be customized from 3000 to 12000 bottles per hour based on requirements.

Versatile Application: Suitable for dry powder and liquid syrup production in 50-500ml plastic or glass bottles.

Global Export Experience: Exported to 45+ countries including Asia, Europe, Middle East, Africa, and South America.

Comprehensive After-Sales Service: Includes 24-hour response, local agent assistance, and engineer dispatch for up to 12 months.

Certified Quality Standards: Equipment designed and manufactured in accordance with GMP, FDA, WHO, ISO, and CE standards.

Flexible Customization Options: Supports full customization, minor customization, and customization from samples or designs.

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: ≤2.89h 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.