Our products meet the highest quality standards. In the first place, our medical oxygen gas and gas cylinder must comply with the regulations of the Dutch Ministry of Health, Welfare and Sports and the European Pharmacopoeia (EP). Both legislations are complementary to each other and are very strict in order to guarantee the integrity of the oxygen gas and the quality of the gas cylinder.
We have set up our supply service in such a way that our products are globally accepted by all the responsible authorities and complies with the guidelines set by the World Health Organization (WHO), International Labour Organization (ILO), the International Maritime Organization (IMO) reflected in the Medical First Aid Guide for use in accidents Involving dangerous Goods (MFAG/IMDG) and the International Medical guide for ships (IMGS). And, of course, is in line with the various Flag State regulations.
Our main goal with this approach is to ensure the integrity of the medical oxygen gas as well as the quality standard of the gas cylinders on a global scale for safe use within the marine & offshore industry. In order to substantiate and guarantee our quality, all our individual MedOx Marine medical oxygen cylinders are supplied with the following documents:
Gas Analysis Certificate
The Gas Analysis Certificate shows the exact values of the gas composition of each batch and can only be provided if the oxygen gas has been produced as a registered medicine. A certificate of conformity is insufficient in our opinion, because this only indicates the minimum values with which the oxygen gas must comply with.
Package Leaflet
The Package Leaflet provides information to the user on the safe use of the gas cylinder, the administration of the oxygen gas, possible side effects and instructions and guidelines for the safe storage of the gas cylinders.
Cylinder Manufacturing & Test Certificate
The Cylinder Manufacturing & Test Certificate shows which production and materials standard has been used in the fabrication of the gas cylinder and that the manufactured gas cylinders have been randomly inspected for irregularities and that they have succesfully passed the pressure test.
MedOx Supply Certificate
The MedOx Supply Certificate states the filling date of the supplied medical oxygen cylinder(s), the most recent hydrostatic test or production date of the cylinder, the batch number(s) of the medical oxygen gas and expiry dates of the medical oxygen gas filling. In addition, the production and end-of-life date of the delivered high pressure regulators are mentioned on the certificate.
Please ensure that you have these documents available in the event of an inspection by Port State Control (PSC), Flag State Control (FSC) or any other inspectorate authority.
The MedOx Portable Resuscitator Set is a handy bag with all the necessities for adequately carrying out resuscitation support. This resuscitator set is part of the basic equipment for every seagoing ship operating more than 200 nautical miles offshore. The MedOx Portable Rescucitator Set contains the following items:
1 MedOx Medical Oxygen Cylinder, 2L, 200 bar, Pin Index, Threaded or Integral
1 HP Reducer with Gauge & Flow Regulator 0 - 25 l/min, Pin Index, Threaded (not applicable for Integral)
1 Guedel Airway, Size 1, 7cm, white, Child
1 Guedel Airway, size 2, 8cm, green, Adult
1 Guedel Airway, size 3, 9cm, orange, Adult
1 Guedel Airway, size 4, 10cm, red, adult
1 Suction Catheter Size Ch12
2 Oxygen Mask, Non-Rebreathing Adult, with tube 2,1m
1 Oxygen Mask, Non-Rebreathing Child, with tube 2,1m
1 Res-Q-Vac Hand Suction Unit
1 Resuscitation Balloon, White, complete set
1 MedOx Bag for Oxygen Set 2L, blue
1 Instruction Leaflet for use Oxygen Set
The consumables inside the Resuscitator Set are also available in refillable MedOx Respiratory Accessory Set.
MedOx Marine works directly with GCE Group in the field of high pressure regulators for medicinal gases marketed under the name GCE Healthcare. GCE Healthcare are committed to the manufacturing of high quality and innovative medical gas equipment and associated accessories. A company known for its unrivalled quality and market-specific expertise. All regulators comply with the Medical Devices Directive and are produced in accordance with EN ISO 9001 and EN ISO 13485.