What payment terms are accepted?

We accept LC, T/T, D/P, PayPal, Western Union, and small-amount payments.

What types of defects can the machine detect?

It detects fiber, hair, white blocks, insoluble objects, bubbles, black spots, and sealing defects.

What is the power source requirement?

The machine operates on AC 380V, 50Hz with a power consumption of 18 KW.

Syrup and Ampoule Bottles

Name: Automated Visual Inspection Machine/High Quality Light Inspection Machine for Vial/Syrup and Ampoule Bottles
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2074688815

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$40,000.00-180,000.00

1 Piece

Product profile

After-sales Service

Engineers Available to Service Machinery Overseas, Free Spare Parts, Online Support, video Technical Support, Field Installation, Commissioning and Training

Analysis Speed

Rapid Analysis

Application

Clinical Diagnosis, Pharmaceutical Industry, Bottle&Bag, Pharmaceutical, Food, Other

Model NO.

Customized IVEN -11

Certification

CE, GMP, ISO

Condition

New

Customized

Detection Range

Metabolites, Proteins, Small Molecules

Material Compatibility

Liquid, Powder

Portability

Machinery

Power Source

Electric Operated

Sensitivity

High Sensitivity

Technology

Nuclear Magnetic Resonance Spectroscopy

User Interface

Touchscreen

Voltage

380V

Capacity

4000-12000bottles/H

Applicable Industries

Manufacturing Plant, Pharmaceutical

Size of Inspection Object

50---1000ml, PP Bottle or Glass Bottle

Inspection Items

Fiber, Hair, White Blocks and Other Insoluble Obj

Compressed Air Consumption

0.6MPa, 0.15m³ /Min

Finished Dosage Form

Liquid

Precision

High Precision

Computerized

Warranty

1 Year

Transport Package

Wooden Case;Inner Water Proof Bag, Outer Sea Worth

Specification

2980*2000*2100 mm

Trademark

IVEN

Origin

China

HS Code

8422303090

Production Capacity

Customized

Key features

High-Speed Inspection: Max capacity up to 18,000 pcs/h with 600 pcs/min speed.

Multi-Station Detection: 10 stations with 23 cameras and 22 light sources for 360-degree sealing and defect inspection.

High Precision Accuracy: Leakage inspection accuracy of 0.3 microns with adjustable voltage 0-22 kv.

Automated Defect Rejection: Automatically eliminates defective products like fibers, hair, and black spots via positive pressure adsorption.

Versatile Bottle Compatibility: Handles 50-1,000ml plastic/PP bottles and 1-20ml ampoules with diameters up to 25mm.

User-Friendly Interface: PLC HMI operation with touch type LCD control panel for easy monitoring.

Easy Maintenance Design: Partial waterproof structure allows direct water washing for broken bottle cleaning.

Comprehensive Certifications: CE, GMP, and ISO certified for pharmaceutical and food industry standards.

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: ≤2.21h 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.