„HYDRO-GAZ-MED” was established in 1971.

Short history of the most important events from HGM history:

  • in 1982 specialization in medical gas pipeline systems;
  • in 1999 implementation of quality assurance system ISO:9002;
  • in 2003 system ISO:9002 was replaced by EN ISO:9001;
  • in 2003 we became authorized and exclusive distributor of GREGGERSEN GmbH in Poland;
  • in 2003 we became authorized and exclusive distributor of  STEPHAN GmbH in Poland;
  • in 2004 our ISO 9001 quality system is replaced by EN ISO:13485 quality system;
  • in 2005 we receive EC Certificate according to Appendix II MDD 93/42;
  • in 2014 we became authorized and exclusive distributor of medical oxygen concentrators of OXYMAT A/S in Poland;
  • w 2015 rozpoczynamy współpracę z jednostką notyfikowaną TÜV NORD.

According to Medical Device Directive 93/42/EC “Medical Gas Pipeline System”  is a class IIb medical device, and as such MUST have CE mark with Notified Body number.

We manufacture, among others, below mentioned devices which we mark with CE 2274:

  • installations and central manifold systems with automatic change over and electronically controlled for:
    • oxygen
    • nitrous oxide
    • carbon dioxide
    • compressed air
    • nitrogen
  • installation and compressor stations for medical compressed air;
  • installations and supply systems for medical vacuum;
  • monitoring and alarm systems for MGPS;
  • medical oxygen concentrator systems for health care facilities;
  • technical documentation for all our works;
  • certification of MGPS medical gas pipeline systems.

We make new installations, modernizations, regular maintenance of MGPS and designing of new systems.
Wa always use newest and most sophisticated solutions in our designs for MGPS. We always use renowned and well known solutions of such manufacturers like OXYMAT A/S, Fritz Stephan GmbH, GREGGERSEN Gasetechnik GmbH and of course our own products.

Each device and material is of course certified for use in medical gas pipeline systems. Our works are done according to EN ISO 7396-1:2016, HTM 2022, EN ISO 13485:2016 and at the end we issue proper declaration of conformity.