[vc_row css=”.vc_custom_1447434872498{margin-top: 20px !important;}”][vc_column][ts_table_data number_column=”2″]Sterilisation of medical devices. Validation and routine control of ethylene oxide sterilisation. | BS EN 550 | 1994

Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment | BS EN 1707 | 1997

Sterilisation of medical devices – Requirements for Medical devices to be labelled sterile | BS EN 556 | 2001

Marking symbols | BS EN 980 | 2008

Anaesthetic and Respiratory  Equipment – Conical Connectors Part 1 Cones and Sockets | BS EN ISO 5356-1 | 2004

Anaesthetic and Respiratory equipment – Heat and Moisture Exchangers (HMES) for humidifying respired Gases in Humans. | ISO 9360 -1 | 2009

Anaesthetic and Respiratory equipment – Heat and Moisture Exchangers for use in humidifying respired Gases in Humans – Part 2: HMES for use with Tracheostomized patients having minimum Tidal volumes of 250 ML  | ISO 9360 -2 | 2009

Biological evaluation of Medical Devices. Part 1 Evaluation and Testing | ISO 10993-1 | 2009

Sterilization of health care products – Ethylene Oxide sterilisation | ISO 11135-1 | 2007

Sterilization of health care products- Radiation | BS EN ISO 11137-2 | 2015

Sterilisation of medical devices – Microbiological Methods – Part 1: Estimation of population of Microorganisms on products  | ISO 11737-1 | 2006

Respiratory protective devices –  Method for test – Part 7: Determination of particle filter penetration | BS EN 13274-7 | 2008

Medical devices – Application of risk management To medical devices | BS EN ISO 14971 | 2012

Medical devices – symbols to be used with medical Device labels, labelling and information to be supplied Part1: General requirements | ISO 15223-1 | 2012

Breathing system filters for anaesthetic and respiratory Use – salt test method to assess filtration performance | BS EN ISO 23328-1 | 2008[/ts_table_data][/vc_column][/vc_row]