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Marya Advanced Wfi Water System for Pharmaceutical Water Injection Production
US$200,000.00
1 Piece
Product profile
Customization
AvailableCertification
ISO9001, RoHS, CESalt Rejection Rate
99.5%Model NO.
Marya AGApplication
IndustryCapacity
200 GallonMachine Power
3.5kwCertificate
CE, ISO, SGSRO Resistivity
up to 15m&Omega.CmRO Microorganisms
≤ 20 Cfu/MlWater Temperature
20-30℃Production Water pH Value
5.0-7.0Power Supply
AC 380VAC 50HzTransport Package
Export Wood CasesSpecification
Standard/customizedTrademark
MaryaOrigin
ChinaKey features
Pharmaceutical Grade Compliance: Meets USP, EP, JP standards and cGMP, FDA, ISPE guidelines for sterile WFI production.
Advanced Purification Tech: Combines RO, distillation, and ultrafiltration for consistent sterile water quality.
Real-time Monitoring: PLC control monitors TOC (<500 ppb), conductivity, and endotoxin levels continuously.
Modular Design: Compact structure enables fast field installation to save time and space.
Flexible Customization: Capacities range from 1,000 to 10,000 L/h with 3D design integration support.
Dual Softener System: Series or parallel design allows alternate resin regeneration and microbial control.
Energy Efficient: Thermal cycling and adjustable RO recovery rates reduce operational costs.
Company profile
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: ≤4.67h
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 standards does the system comply with?
A:
The system meets USP, EP, and JP stringent standards and complies with cGMP, FDA, and ISPE guidelines.
Q:Can the production capacity be customized?
A:
Yes, customizable capacities range from 1,000 to 10,000 L/h with 3D design integration.
Q:What purification technologies are used?
A:
It employs multi-stage purification including reverse osmosis (RO), distillation, and ultrafiltration.
Q:What is the minimum order quantity?
A:
The minimum order quantity is 1 Set.
Q:Do you offer OEM and ODM services?
A:
Yes, both OEM and ODM services are available with full and flexible customization options.
Send Inquiry
*To:
Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.
Shanghai Marya Pharmaceutical Engineering & Project Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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