How does the machine handle defective products?

It uses a positive pressure adsorption rejection device to automatically send unqualified products to a separate line.

What after-sales services are provided?

We offer field installation, commissioning, training, and 24-hour on-call technical support throughout the year.

What is the minimum order quantity?

The minimum order quantity is 1 set.

GMP Standard Small Bottle Visual Inspection Machine/ Automatic Visual Inspection Equipment for Pharmaceutical & Medical Industry

Name: GMP Standard Small Bottle Visual Inspection Machine/ Automatic Visual Inspection Equipment for Pharmaceutical & Medical Industry
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2061892625

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$50,000.00-600,000.00

1 Piece

Product profile

Application

Chemical Industry, Pharmaceutical Industry, Bottle&Bag, Pharmaceutical, Food, Other

Automation Grade

Automatic

Features

Sterilization Capability, Vacuum Packaging

Model NO.

Customized IVEN -1

Machine Material

Stainless Steel

Packaging Material

Plastic, PVC

Warranty

1 Year

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

Certification

CE, GMP, ISO

Voltage

380V

Computerized

Customized

Condition

New

After-Sales Service

Field Installation, Commissioning and Training

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 inspection stations with 23 cameras and 22 light sources.

Advanced AI Technology: Deep machine learning and ultrasonic defoaming for precision.

GMP & CE Certified: Meets GMP standards with CE, ISO certifications for safety.

Customizable Capacity: Capacity adjustable from 4,000 to 12,000 bottles per hour.

24/7 After-Sales Support: 24-hour on-call service with field installation and training.

Versatile Application: Inspects 50-1000ml plastic/glass bottles, ampoules, and vials.

Smart Rejection System: Automatically rejects defects via positive pressure adsorption.

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: ≤1.72h 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.