What are the payment terms?

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

What is the lead time for production?

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

What certifications does the machine have?

The machine is certified with CE and meets GMP standards.

Xgf PP Bottle Lvp Wash-Fill-Seal Machine with GMP Standard

Name: Xgf PP Bottle Lvp Wash-Fill-Seal Machine with GMP Standard
Brand: Shanghai Iven Pharmatech Engineering Co., Ltd.
SKU: 2072117895

Shanghai, ChinaShanghai Iven Pharmatech Engineering Co., Ltd.

US$180,000.00-400,000.00

1 Piece

Product profile

After-sales Service

Video Technical Support,Field Maintenance and Repa

Warranty

1 Year

Automatic Grade

Fully Automatic

Model NO.

customized

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

Applicable Industries

Manufacturing Plant, Pharmaceutical

Feature

Durable,Quick Changeover

Filling Volume

50 - 5000 Ml

Filling Accuracy

±2%

Machinery Capacity

2000bph

Weight

3--12t, 3-12t

Driven Type

Electric

Filling Material

Water

Transport Package

Wooden Case; Wooden Package;

Specification

6500*4300*3500 mm

Trademark

IVEN

Origin

China

Key features

GMP Standard Compliance: Complete cleaning and sterilization function compliant with GMP standards.

High Production Capacity: Capacities up to 15,000 BPH depending on customer request and bottle size.

Precise Filling Control: Accurate air discharging controls bottle deformation after sterilization.

Advanced PLC Control: PLC system allows setting, changing, and storing all operation data.

Flexible Customization: Supports customization from samples, designs, and minor adjustments.

Multi-Head Configuration: Multi-head filling and sealing for efficient rotary processing.

Safety & Alarm System: Voice alarm and machine halt upon fault detection for 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: ≤2.00h 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.