With a consolidated know-how, Cobams offers its many years of experience in the supply of solutions and devices for neonatal intensive care. We manufactur equipment for continuous monitoring of vital signs in the newborn .

Infant Incubator
Transport Incubator
Infant Warmer
Phototherapy Apparatus
Warmer Unit

Production

The production of the equipment involve numerous steps and organisations . Cobams ensure the highest possible quality control standards . Quality control pass through a carefully controlled series of main inspections undertaken by professional employments trained for this task.

Delivery

Each unit is identified with all references and marked for easy identification on arrival at the final destination.

Installation

Qualified technicians provide to the onsite installation of the equipment delivered. The installation technician and the site manager can offer to users a guarantee of perfect operation .

SALES AND MARKETING

Export to over 45 foreign countries offering sales service and after-sales service. Besides the wide range and competitive prices, Cobams achieved great success with trade marketing activities, focusing on technical point of sale and reduced delivery times.

INTERNATIONAL EXHIBITION

COBAMS will exhibit at Medica Dusseldorf and Arab Health Dubai alongside over 5,000 of the world`s top medical device companies, distributors and other key decision makers in the healthcare sector.

QUALITY SYSTEM AND PRODUCT CERTIFICATION

Since 1968 we produce with constant reference to the requirements of Quality & Safety ISO9001:2015 Quality management systems

COBAMS demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and aims to enhance customer satisfaction through the effective application of the system, including processes for improvement of the system and the assurance of conformity to customer and applicable statutory and regulatory requirements.

ISO 13485:2016 Medical devices -- Quality management systems
COBAMS manage all processes under the ISO 13485:2016 providing medical devices including application of system by monitoring, maintaining, and controlling the processes.

European Directive 93/42/EEC _ CE0476
Medical Device Directive 93/42/EEC(MDD) lists the Essential Requirements on safety, efficacy and quality performances that a medical device must meet.

UNI EN 1789 CRASH TEST 10g
COBAMS conducted the crush-tes 10 g test to determine if the maintain systems (restraint systems) and the fixation of the equipment ( transport incubator code 002/002S ) meets the requirements specified under UNI EN 1789 and UNI EN 1865

Cobams Album - Video