Sourcing medical equipment, hospital supplies, and healthcare consumables from China and Asia — with the certification verification, quality control, and documentation that patient safety demands.
Plutonia sources medical and laboratory products with the diligence that patient safety demands — verified certifications, traceable supply chains, and documentation that satisfies regulatory bodies.
Hospital beds, ward furniture, operating tables, examination couches, trolleys, lockers, and patient room equipment. CE and ISO 13485 verified manufacturers.
Ultrasound machines, X-ray systems, ECG monitors, laboratory analysers, blood pressure monitors, pulse oximeters, and point-of-care diagnostics.
General surgical sets, laparoscopic instruments, orthopaedic tools, sterilisation equipment, and surgical consumables from ISO 13485 certified manufacturers.
Medical gloves (nitrile, latex), surgical masks, N95/FFP2/FFP3 respirators, isolation gowns, face shields, disinfectants, and sterilisation products.
Laboratory plasticware, culture media, diagnostic reagents, pipettes, centrifuge tubes, and analytical consumables for clinical and research laboratories.
GMP-certified pharmaceutical procurement, vaccine cold chain equipment (refrigerators, cold boxes), blood storage units, and temperature-controlled logistics.
Medical oxygen concentrators, cylinders, manifold systems, ventilators, CPAP/BiPAP machines, and anaesthesia equipment for hospitals and clinics.
Emergency trolleys, defibrillators, portable monitors, trauma kits, ambulance equipment, stretchers, and first response medical supplies.
Digital X-ray, mobile radiology units, mammography equipment, and imaging accessories — with radiation safety documentation and CE/FDA registration verification.
Every medical product we source is evaluated against the certification requirements of the destination market. We coordinate verification with issuing bodies — not just document review.
European conformity marking under the Medical Device Regulation. Required for all medical devices entering the EU and many other markets. We verify CE certificates against the issuing Notified Body and confirm current validity.
US Food and Drug Administration registration for medical devices. We verify 510(k) clearance numbers through the FDA device database and confirm the specific device model is registered, not just the manufacturer.
International standard for Quality Management Systems in medical device manufacturing. ISO 13485 certification indicates the factory has documented QMS — but does not certify the specific product. We audit the QMS separately.
National Agency for Food and Drug Administration and Control registration required for medical products entering Nigeria. We coordinate NAFDAC registration and SONCAP certification for health products destined for Nigeria.
Saudi Food and Drug Authority registration and SASO conformity certification for medical devices entering the Kingdom of Saudi Arabia. We manage the SALEEM program registration process for applicable devices.
WHO PQ required for medicines and medical devices procured under WHO, UNICEF, GAVI, and Global Fund programs. We source from WHO prequalified manufacturers and verify prequalification status for each specific product.
CE, FDA, ISO, IEC, UKCA, NAFDAC, SFDA, WHO, GMP and GDP names and marks are the property of their respective standards and regulatory bodies. They are shown to indicate the certification standards Plutonia verifies suppliers against and coordinates documentation for on behalf of clients — not to imply that Plutonia issues these certifications, nor any endorsement, accreditation, or affiliation. Final regulatory acceptance depends on destination-market requirements and the relevant authorities.
Hospital emergencies, epidemic response, and humanitarian health crises do not wait for standard procurement timelines. We operate a dedicated emergency track for time-critical medical supply.
Submit your requirement with product specifications, quantity, and destination. Our team immediately draws on our pre-verified medical equipment network to identify available stock and production capacity. Air freight is arranged within hours of order placement, with documentation prepared in parallel with production.
We have executed emergency medical procurement for hospitals, government health ministries, and NGO emergency response programs across Africa, the Middle East, and Asia.
We review your product specification, certification requirements, quantity, destination, and timeline.
We identify ISO 13485 certified manufacturers with the relevant CE, FDA, or market-specific certification for your product.
All certifications are verified directly with issuing bodies — CE certificates with Notified Bodies, FDA numbers through the official database.
Pre-shipment inspection by qualified QC inspectors verifying product specifications, packaging, labelling, and documentation completeness.
Freight arranged with medical equipment experience. Full documentation package prepared for customs clearance and regulatory compliance at destination.
Tell us your requirement — product, quantity, destination, certifications needed. We respond to serious inquiries within one business day.