What is the minimum order quantity?

The minimum order quantity is 1 set, allowing for flexible purchasing for various project scales.

What are the lead times for production?

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

Marya 316L Stainless Steel Liquid Preparation System Featuring 3D Simulation & Electromagnetic Stirrer

Name: Marya 316L Stainless Steel Liquid Preparation System Featuring 3D Simulation & Electromagnetic Stirrer
Brand: Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.
SKU: 1967295961

Shanghai, ChinaShanghai Marya Pharmaceutical Engineering & Project Co., Ltd.

US$50,000.00

1 Piece

US$40,000.00

2+ Pieces

Product profile

Customization

Available

Application

Biotechnology Industry, Chemical industry, Clinical Diagnosis, Food & Beverage Factory, Food Safety, Forensic Science, Pharmaceutical Industry

Capacity

20000 L/hr

Certification

CE, FDA, GMP, ISO

Control System

Fully Automatic

Treatment Process

Filtration, Ultrafiltration

Warranty of core components

1 Year

Power Supply

380V 50Hz

Tank Material

Stainless Steel 316L

Weighing Control Accuracy

Sealing and Protection Levels

IP65

Temperature Control Accuracy

Temperature Range-10~150℃ ±0.2℃

Stirring Speed Control Accuracy

Speed Range 0~450rpm ±3.0%

Temperature Resistance

150℃

Transport Package

Wooden Box

Specification

350*180*300

Trademark

Marya

Origin

China

Key features

Fully Automated Operation: Features 1-click CIP/SIP, recipe management, e-signatures, and audit trails for full automation.

3D Simulation Design: Pre-production 3D modeling optimizes piping and valve placement for ergonomic and user-friendly operation.

Modular Cost-Saving Design: Pre-tested modular equipment reduces installation costs, accelerates delivery, and ensures flexibility.

Precise Process Control: Real-time monitoring of temp, DO, pH with auto-alerts to ensure drug quality and consistency.

High-Performance Filtration: Sterilization-grade PES filters with organic solvent compatibility and reliable bacterial retention.

Versatile Stirring Options: Offers upper mechanical or lower magnetic stirring with variable frequency speed regulation.

Sterility Assurance: Includes sterile ventilation filters and CIP spray balls for aseptic operations and cleanability.

Company profile

Flexible CustomizationProduct CertificationYears of Export ExperienceR&D Capabilities

Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.

Shanghai, China

CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service Available CertifiedCustomization Options: Full Customization, Flexible customization CertifiedExport Year: 12 Years CertifiedNearest Port: Shanghai Port; Ningbo PortAverage Response Time: ≤4.24h

About Our Factory & Business Background

AddressNo211, North Fute Road, Pudong Area, 200131, Shanghai, China

Plant Area3210 square meters

Number of Employees69

Terms of PaymentLC, T/T, D/P, PayPal, Western Union, Small-amount payment, Money Gram

International Commercial Terms(Incoterms)FOB, EXW, CFR, CIF, DDP, CIP, Others

Average Lead TimePeak Season Lead Time: 1-3 months Off Season Lead Time: one month

Minimum Order Quantity1 Set

Supply Chain Partners150

Our Production Capability & Technical Expertise

Main ProductsPharmaceutical Filling Line, Cleanroom Project

Production Lines6

Production MachinesWelding Machine, Lathe, Milling Machine, Bench Drill

QA/QC inspectors3 people

Inspection Type for Finished Products100% inspection(Visual inspection & Function inspection)

Inspection Method for Finished ProductsHave instructions and uniformly followed

R&D Engineers30 people

Traceability of Raw MaterialsYes

Our Industry Experience & Global Business Record

Year of Establishment2014-03-10

Main MarketsNorth America, South America, Eastern Europe, Southeast Asia, Africa, Oceania, Mid East, Eastern Asia, Western Europe

Repeat Buyers Choice10%~30%

Number of Foreign Trading Staff16

Overseas Agent/BranchNo

New Products Launched in Last yearYes

Our Certifications, Standards & Industry Recognition

Product CertificationCE

Cooperated with Fortune 500Yes

Product Q&A

Q:What is the working volume capacity?

The working volume ranges from 2L to 15,000L, accommodating various production scales from small-batch to large-volume parenteral solutions.

Q:Is the system fully automated?

Yes, it features fully automated operation including 1-click CIP/SIP, computerized recipe management, e-signatures, e-records, and audit trails for compliance.

Q:What certifications does the equipment have?

The system is certified with CE, FDA, GMP, and ISO standards, ensuring compliance with international pharmaceutical manufacturing regulations.

Q:Can the system be customized?

Yes, full customization and flexible customization options are available, including power supply, tank material, and specific control accuracies.

Q:What is the warranty period for core components?

The warranty for core components is 1 year, covering mechanical defects with free parts and labor.