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Lds1000L/H-6 Wemac Best Multi-Effect Water Machine for Pharma Industy Injectable Water
US$25,000.00-32,000.00
1 Piece

Product profile

Application

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

Capacity

1000L/H

Certification

CE, FDA, GMP, ISO

Model NO.

LDS1000-6

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

1000L/H

Trademark

WEMAC

Origin

China

HS Code

8419409090

Production Capacity

1000L/H

Key features

SS316L Material Construction: All parts contacting water use SS316L with electrochemical polishing for smoothness.
Multi-Effect Energy Saving: Uses secondary steam step-by-step; 6-effect model requires no cooling water.
Pharmacopoeia Compliance: Meets WFI requirements of CP2020, USP43, and EP10 standards.
Fully Automatic Control: HMI+PLC system with simple interface and at least three authority levels.
Customizable Size: Size is customized to meet specific project requirements.
Advanced Separation Tech: Three-stage separation: falling film, gravity, and spiral flow.
Certified Quality: Holds CE, FDA, GMP, and ISO certifications for global compliance.
Comprehensive Documentation: Provides endoscopic photos, solder diagrams, and passivation reports.

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:
Option 1: Engineers visit for commissioning (travel and labor costs borne by buyer). Option 2: Online service with free parts if under warranty (shipping costs borne by buyer).
Q:How long is the warranty period?
A:
The warranty period for the entire storage tank, main equipment, accessories, and auxiliary equipment is 1 year.
Q:What materials are used for the water distiller?
A:
All parts in contact with raw water, water for injection, and secondary pure steam are made of SS316L.
Q:Does the equipment meet international pharmacopoeia standards?
A:
Yes, the produced water for injection meets requirements of Chinese Pharmacopoeia (CP2020), United States Pharmacopoeia (USP43), and European Pharmacopoeia (EP10).

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