Invoice # | Invoice Date |
---|---|
Sterilisation of medical devices. Validation and routine control of ethylene oxide sterilisation. | BS EN 550 |
Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment | BS EN 1707 |
Sterilisation of medical devices – Requirements for Medical devices to be labelled sterile | BS EN 556 |
Marking symbols | BS EN 980 |
Anaesthetic and Respiratory Equipment – Conical Connectors Part 1 Cones and Sockets | BS EN ISO 5356-1 |
Anaesthetic and Respiratory equipment – Heat and Moisture Exchangers (HMES) for humidifying respired Gases in Humans. | ISO 9360 -1 |
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 |
Biological evaluation of Medical Devices. Part 1 Evaluation and Testing | ISO 10993-1 |
Sterilization of health care products – Ethylene Oxide sterilisation | ISO 11135-1 |
Sterilization of health care products- Radiation | BS EN ISO 11137-2 |
Sterilisation of medical devices – Microbiological Methods – Part 1: Estimation of population of Microorganisms on products | ISO 11737-1 |
Respiratory protective devices – Method for test – Part 7: Determination of particle filter penetration | BS EN 13274-7 |
Medical devices – Application of risk management To medical devices | BS EN ISO 14971 |
Medical devices – symbols to be used with medical Device labels, labelling and information to be supplied Part1: General requirements | ISO 15223-1 |
Breathing system filters for anaesthetic and respiratory Use – salt test method to assess filtration performance | BS EN ISO 23328-1 |