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Lds6000L/H-6 Pharmacopoeia Grade Wfi Generator: Multi-Effect Distillation
US$60,000.00-69,000.00
1 Piece

Product specifications

Capacity

Product profile

Application

Biotechnology Industry, Chemical industry, Food & Beverage Factory, Pharmaceutical Industry

Capacity

6000L/H

Certification

CE, FDA, GMP, ISO

Model NO.

LDS6000L/H-6

Control System

Fully Automatic

Treatment Process

Chlorination, Electrodeionization, Filtration, Ozonation, Reverse Osmosis, Softening, Ultrafiltration, UV Disinfection

Warranty of core components

1 Year

Material

SS316L

Machinery Test Report

Provided

Electrical Equipment

Siemens(Germany)

Size

Customized

Recording Method

Electronic Recording/Paperless

Transport Package

Wooden

Specification

6000L/H

Trademark

WEMAC

Origin

China

HS Code

8419409090

Production Capacity

5000sets Per Year

Key features

Pharmacopoeia Compliance: Meets WFI standards in Chinese (CP2020), US (USP43), and European (EP10) Pharmacopoeias.
High Energy Efficiency: Uses secondary steam step-by-step; six-effect model requires no cooling water.
Premium SS316L Material: All parts contacting water/steam are made of SS316L with electrochemical polishing.
Customizable Size: Size is customized to meet specific project requirements.
Advanced Control System: HMI+PLC fully automatic control with at least three authority levels.
Anti-Contamination Design: Double tube sheets and expanded welding prevent cross-contamination.
Comprehensive Certification: Certified by CE, FDA, GMP, and ISO for global market compliance.
60 Years Experience: Over 60 years of specialized experience in pharmaceutical water equipment.

Company profile

Business Type: Manufacturer/Factory, Trading Company CertifiedR&D Capacity: ODM Service Available & OEM Service AvailableAverage Response Time: ≤1.45h

AI-Powered supplier vetting

SummaryThe supplier is identified as a trading company with biomass energy-related technical services in its stated business scope. It reports OEM and ODM capabilities, sample- and design-based customization, four production lines, and 50 quality-control staff. Export-related evidence is mixed: one slice states 41%–50% of sales come from exports and exports through agents and self-operated import/export rights, while another identifies the primary market as domestic and a separate slice states no overseas service locations or overseas agents. Service-management documentation is weak, with no written procedures or records for supplier assessment, corrective actions, or complaint handling. No SDK, no new products in the past year, and only two years of R&D engineer experience are reported. Financial and sustainability evidence is insufficient for a firm assessment, while customer-case evidence indicates validation-document experience and exports to more than 40 countries and regions.
After-Sales capabilityAfter-sales and service-management controls appear weak: there are no written procedures or records for service-capability assessment, corrective and preventive actions, or complaint handling. The supplier also reports no overseas warehouse, showroom, agent, branch, or offline trade-show capability, although it lists acceptable service terms and 13 qualified suppliers; these do not establish effective after-sales support.
R&D capabilityThe supplier reports ODM service and customization from samples and designs, but no available SDK, no new products during the past year, and only two years of total R&D-engineer experience. These explicit limitations outweigh the stated ODM capability for an overall innovation assessment.
Production capacityThe supplier reports four production lines, 50 quality-control staff, and combined facilities including flatting, cutting, and automatic welding machines. However, finished-product inspection has instructions but no written records, so production resources are demonstrated while process-documentation control is incomplete.
Customization capabilityBoth slices explicitly report customization from samples and from designs, and the supplier also states that it provides ODM services. This directly supports a demonstrated ability to handle customized products.
Client casesThe supplier states that its sales volume ranks first in China, that it has exported to more than 40 countries and regions, and that it has provided pharmaceutical validation documents including DQ, IQ, OQ, PQ, FAT, and SAT. These statements provide explicit evidence of broad market reach and sector-relevant customer experience, although no individual customer names are given.

Product Q&A

Q:How many years of experience do you have in pharmaceutical water equipment?
A:
We have over 60 years of experience in pharmaceutical water equipment.
Q:What are the installation options?
A:
We offer two options: 1) On-site commissioning by our engineers (travel and labor costs borne by buyer); 2) Online services with free parts during warranty (shipping costs borne by buyer).
Q:What is the warranty period?
A:
The warranty period for the entire storage tank, main equipment, accessories, and auxiliary equipment is 1 year.
Q:Which pharmacopoeias does the WFI meet?
A:
The WFI produced meets the requirements of Chinese Pharmacopoeia (CP2020), United States Pharmacopoeia (USP43), and European Pharmacopoeia (EP10).
Q:What material is used for water contact parts?
A:
All parts in contact with raw water, water for injection, and secondary pure steam are made of SS316L.

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*To:Shandong Eagle Water Treatment Technology Co.,Ltd
*Content:
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