logo
Welcome to Jiangsu Luoming Purification Technology Co., Ltd.
+8615850254955

ISO13485 Medical Device PSA Oxygen Generator 30Nm3/h 93% Purity CE Certified for Hospital Procurement

Basic Properties
Place of Origin: Jiangsu, China
Brand Name: LuoMing
Certification: ISO 13485, ISO 9001, CE
Model Number: LMO-30
Trading Properties
Minimum Order Quantity: 1 Set
Price: USD 40,000-100,000 / Set
Payment Terms: T/T,L/C
Supply Ability: 60 Sets per Month
Product Summary
ISO 13485 medical device certified PSA oxygen generator producing 93%±3% purity at 30Nm3/h, designed for large-scale hospital tenders with complete regulatory documentation package ensuring rapid customs clearance and local health authority approval.

Product Details

Highlight:

ISO13485 Medical Device O2 Generator

,

CE Certified Hospital Oxygen Plant

,

Tender Ready PSA Oxygen System

Oxygen Flow Rate: 30Nm3/h
Oxygen Purity: 93%±3%
Outlet Pressure: 0.4-0.6 MPa
Technology: Pressure Swing Adsorption (PSA)
Certification: ISO 13485, ISO 9001, CE
Quality System: Medical Device Quality Management System
Documentation: Full Tender Package, CE DoC, ISO Certificates, FAT Reports
Operation Mode: PLC Fully Automatic With Remote Monitoring
Power Supply: 380V/50Hz/3Phase (Customizable)
Service Life: 10+ Years
After-Sales Service: Video Technical Support, Online Support, Field Service Available
Product Description
ISO13485 Medical Device PSA Oxygen Generator 30Nm³/h 93% Purity CE Certified for Hospital Procurement
Medical Oxygen Generator Overview

The PSA Medical Oxygen Generator is purpose-built for large-scale hospital procurement and government healthcare infrastructure projects. Manufactured under Luoming's ISO 13485 medical device quality management system with ISO 9001 and CE certifications, this 30Nm³/h system delivers 93% ±3% medical-grade oxygen with complete regulatory documentation—eliminating compliance risks and accelerating project timelines from purchase order to operational handover.

Built for Tender Success - Compliance From Day One

Hospital and government procurement increasingly mandate ISO 13485 certification and CE marking as non-negotiable prequalification criteria. Our system meets and exceeds these requirements. The ISO 13485 certification covers the entire product lifecycle—design, manufacturing, testing, packaging, and post-market surveillance—giving tender evaluation committees the documented evidence they need to approve your bid. With a comprehensive technical dossier, CE Declaration of Conformity, factory audit reports, and third-party test records included as standard, this system transforms regulatory compliance from a procurement bottleneck into a competitive advantage.

Streamlined Regulatory Acceptance Across Borders

One of the biggest challenges in international medical device trade is navigating diverse regulatory landscapes. Our system addresses this with a universal compliance framework built on ISO 13485 and CE certification—two standards recognized or harmonized by health authorities in Europe, the Middle East, Southeast Asia, Africa, and Latin America. Each shipment includes a pre-assembled regulatory package: ISO certificates with accredited body verification, CE for EU market access, material and component traceability records, factory acceptance test (FAT) reports, and installation qualification (IQ) and operational qualification (OQ) templates. For local health authorities, this means faster document review, fewer clarification requests, and confidence in issuing operational permits for the installed system.

30Nm³/h Capacity - Serving Medium to Large Hospitals

With an oxygen output of 30Nm³/h at 93%±3% purity, this system is sized to meet the demands of medium to large hospitals with 200-500 beds, covering central pipeline supply to wards, ICUs, operating theaters, and emergency departments simultaneously. The PSA twin-tower design with PLC automatic control ensures uninterrupted 24/7/365 operation. Built-in remote monitoring capability allows hospital engineering teams and Luoming's after-sales support to track system status in real time, enabling predictive maintenance and rapid response—critical features that further strengthen tender technical evaluation scores.

Key Features
  • ISO 13485 Medical Device Certified: Design, production, and servicing under audited quality management system
  • CE Marked with Full DoC: Complete conformity documentation for EU and harmonized markets
  • ISO 9001:2015 Certified: Enterprise-wide quality management across all functions
  • Tender-Ready Documentation: Pre-assembled regulatory package reduces bid preparation time
  • 30Nm³/h Capacity: Suitable for 200-500 bed hospitals with central pipeline supply
  • Global Recognition: Certifications accepted by health authorities across Europe, MENA, ASEAN, and Africa
  • FAT Reports Included: Factory acceptance test data validates performance before shipment
  • Remote Monitoring Capable: Networked PLC enables real-time oversight and predictive maintenance
Technical Specifications
Parameter Specification
Model LMO-10
Oxygen Flow Rate 30 Nm³/h
Oxygen Purity 93%±3%
Outlet Pressure 0.4-0.6 MPa
Technology Pressure Swing Adsorption (PSA)
Certifications ISO 13485, ISO 9001, CE
Control System PLC Fully Automatic with Remote Monitoring
Power Supply 380V / 50Hz / 3 Phase
Documentation Full Tender Package, FAT Reports, CE DoC
Suitable Hospital Size 200-500 Beds
About Jiangsu Luoming Purification Technology Co., Ltd

Located in Yancheng City, China, Luoming Purification Technology is an ISO 13485 and ISO 9001 certified manufacturer specializing in air separation and medical gas generation equipment. With a track record of supplying hospitals and healthcare projects across 50+ countries, Luoming understands the regulatory demands of international medical device procurement. Our commitment to quality is embedded in our certifications: every process from raw material sourcing to final shipment is documented, auditable, and compliant. We provide our global partners not just equipment, but a complete regulatory pathway to operational deployment.

Frequently Asked Questions
Can you provide documentation for government tender submissions?
Yes. We provide a complete tender support package including ISO 13485 and ISO 9001 certificates, CE Declaration of Conformity, company registration documents, factory audit reports, product technical specifications, and FAT report templates. We can tailor documentation to meet specific tender requirements.
How do your certifications speed up customs clearance?
ISO 13485 and CE certificates are internationally recognized quality indicators. Customs authorities in many countries expedite clearance for products with these certifications because they demonstrate compliance with established safety and quality standards, reducing the need for additional inspections.
What happens if local health authorities need additional documentation?
Our regulatory team can provide supplementary documentation including detailed material certifications, electrical safety test reports, pressure vessel certifications, and any other country-specific requirements. We support our clients throughout the entire regulatory approval process.
Is the system suitable for tenders requiring pre-shipment inspection?
Yes. We welcome third-party inspection agencies such as SGS, Bureau Veritas, and TÜV to conduct pre-shipment inspections at our factory. Our ISO 13485 quality system ensures full traceability and documentation readiness for any inspection scope.
Related Products

Send An Inquiry