| BS EN 28872:1993 | Aluminium caps for transfusion, infusion and injection bottles. General requirements and test methods | Withdrawn |
| BS EN ISO 8872:2003 | Aluminium caps for transfusion, infusion and injection bottles. General requirements and test methods | Current |
| BS EN 1707:1997 | Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment. Lock fittings | Current |
| BS EN 20594-1:1994 | Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - General requirements | Current |
| BS 3930-2:1991 | Conical fittings with a 6% (Luer) taper for syringes, needles and other medical equipment - Specification for lock fittings | Withdrawn |
| BS ISO 11418-1:2005 | Containers and accessories for pharmaceutical preparations - Drop-dispensing glass bottles | Current |
| BS ISO 11418-2:2005 | Containers and accessories for pharmaceutical preparations - Screw-neck glass bottles for syrups | Current |
| BS ISO 11418-3:2005 | Containers and accessories for pharmaceutical preparations - Screw-neck glass bottles (veral) for solid and liquid dosage forms | Current |
| BS ISO 11418-4:2005 | Containers and accessories for pharmaceutical preparations - Tablet glass bottles | Current |
| BS ISO 15010:1998 | Disposable hanging devices for transfusion and infusion bottles. Requirements and test methods | Current |
| BS EN ISO 8871:1997 | Elastomeric parts for aqueous parenteral preparations | Withdrawn |
| BS EN ISO 8871-1:2004 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Extractables in aqueous autoclavates | Current |
| BS EN ISO 8871-2:2004 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Identification and characterization | Current |
| BS EN ISO 8871-4:2006 | Elastomeric parts for parenterals and for devices for pharmaceutical use - Biological requirements and test methods | Current |
| BS EN ISO 8871-3:2004 | Elastomeric parts for parenterals and for devices for pharmaceuticals use - Determination of released-particle count | Current |
| BS ISO 23500:2011 | Guidance for the preparation and quality management of fluids for haemodialysis and related therapies | Current, Work in Hand |
| BS EN 1283:1996 | Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits | Current |
| BS ISO 15375:2004 | Hanging devices for multiple use with infusion bottles. Requirements and test methods | Withdrawn |
| BS EN ISO 8536-2:2002 | Infusion equipment for medical use - Closures for infusion bottles | Withdrawn |
| BS EN ISO 8536-8:2004 | Infusion equipment for medical use - Infusion equipment for use with pressure infusion apparatus | Current |
| BS EN ISO 8536-9:2004 | Infusion equipment for medical use - Fluid lines for use with pressure infusion equipment | Current |
| BS EN ISO 8536-10:2004 | Infusion equipment for medical use - Accessories for fluid lines for use with pressure infusion equipment | Current |
| BS EN ISO 8536-11:2004 | Infusion equipment for medical use - Infusion filters for use with pressure infusion equipment | Current |
| BS EN ISO 8536-3:1999 | Infusion equipment for medical use - Aluminium caps for infusion bottles | Withdrawn |
| BS EN ISO 8536-2:1999 | Infusion equipment for medical use - Closures for infusion bottles | Withdrawn |
| BS EN ISO 8536-1:1999 | Infusion equipment for medical use - Infusion glass bottles | Withdrawn |
| BS EN ISO 8536-1:2011 | Infusion equipment for medical use - Infusion glass bottles | Current |
| BS EN ISO 8536-2:2010 | Infusion equipment for medical use - Closures for infusion bottles | Current |
| BS EN ISO 8536-4:2010 | Infusion equipment for medical use - Infusion sets for single use, gravity feed | Withdrawn |
| BS EN ISO 8536-3:2009 | Infusion equipment for medical use - Aluminium caps for infusion bottles | Current |
| BS EN ISO 8536-4:2004 | Infusion equipment for medical use - Infusion sets for single use, gravity feed | Withdrawn |
| BS EN ISO 8536-1:2003 | Infusion equipment for medical use - Infusion glass bottles | Withdrawn |
| BS EN ISO 8536-4:2007 | Infusion equipment for medical use - Infusion sets for single use, gravity feed | Withdrawn |
| BS EN ISO 8536-1:2008 | Infusion equipment for medical use - Infusion glass bottles | Withdrawn |
| BS EN ISO 8536-5:2011 | Infusion equipment for medical use - Burette infusion sets for single use, gravity feed | Withdrawn |
| BS EN ISO 8536-5:2013 | Infusion equipment for medical use - Burette infusion sets for single use, gravity feed | Current |
| BS EN ISO 8536-4:2013 | Infusion equipment for medical use - Infusion sets for single use, gravity feed | Current |
| BS ISO 8536-7:2009 | Infusion equipment for medical use - Caps made of aluminium-plastics combinations for infusion bottles | Current |
| BS EN ISO 8362-4:2011 | Injection containers and accessories - Injection vials made of moulded glass | Current |
| BS EN ISO 8362-7:2010 | Injection containers and accessories - Injection caps made of aluminium-plastics combinations without overlapping plastics part | Current |
| BS EN ISO 8362-2:2010 | Injection containers and accessories - Closures for injection vials | Current |
| BS EN ISO 8362-1:2009 | Injection containers and accessories - Injection vials made of glass tubing | Current |
| BS EN ISO 8362-6:2011 | Injection containers and accessories - Caps made of aluminium-plastics combinations for injection vials | Current |
| BS EN ISO 8362-3:2003 | Injection containers and accessories - Aluminium caps for injection vials | Current |
| BS EN ISO 8362-4:2004 | Injection containers and accessories - Injection vials made of moulded glass | Withdrawn |
| BS EN ISO 8362-1:2004 | Injection containers and accessories - Injection vials made of glass tubing | Withdrawn |
| BS EN 28362-3:1993 | Injection containers for injectables and accessories - Aluminium caps for injection vials | Withdrawn |
| BS EN 28362-2:1993 | Injection containers for injectables and accessories. - Closures for injection vials | Withdrawn |
| BS EN 28362-4:1993 | Injection containers for injectables and accessories. - Injection vials made of moulded glass | Withdrawn |
| BS EN 28362-1:1993 | Injection containers for injectables and accessories. - Injection vials made of glass tubing | Withdrawn |
| BS EN ISO 9187-1:1999 | Injection equipment for medical use - Ampoules for injectables | Withdrawn |
| BS EN ISO 9187-2:1999 | Injection equipment for medical use - One-point-cut (OPC) ampoules | Withdrawn |
| BS EN ISO 9187-1:2010 | Injection equipment for medical use - Ampoules for injectables | Current |
| BS EN ISO 9187-2:2010 | Injection equipment for medical use - One-point-cut (OPC) ampoules | Current |
| BS EN ISO 9187-1:2008 | Injection equipment for medical use - Ampoules for injectables | Withdrawn |
| BS EN ISO 9187-1:2003 | Injection equipment for medical use - Ampoules for injectables | Withdrawn |
| PD CR 13825:2000 | Luer connectors. A report to CEN CHeF from the CEN forum task group 'Luer fittings' | Current |
| BS ISO 28620:2010 | Medical devices. Non-electrically driven portable infusion devices | Current |
| BS EN 60601-2-41:2009+A11:2011 | Medical electrical equipment - Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis | Current, Work in Hand |
| BS EN 60601-2-16:1998 | Medical electrical equipment. Particular requirements for safety - Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment | Current, Work in Hand |
| BS EN 60601-2-39:1999 | Medical electrical equipment. Particular requirements for safety - Particular requirements for safety. Specification for peritoneal dialysis equipment | Withdrawn |
| BS EN 60601-2-24:1998 | Medical electrical equipment. Particular requirements for safety - Particular requirements for the safety of infusion pumps and controllers | Current, Work in Hand |
| BS EN 50072:1992 | Medical electrical equipment. Particular requirements for safety. Specification for peritoneal dialysis equipment | Withdrawn |
| BS ISO 15375:2010 | Medical infusion bottles. Suspension devices for multiple use. Requirements and test methods | Current |
| BS EN ISO 21649:2009 | Needle-free injectors for medical use. Requirements and test methods | Current |
| BS EN ISO 21649:2006 | Needle-free injectors for medical use. Requirements and test methods | Withdrawn |
| BS EN ISO 15747:2005 | Plastic containers for intravenous injection | Withdrawn |
| BS EN ISO 15747:2010 | Plastic containers for intravenous injections | Withdrawn |
| BS EN ISO 15747:2011 | Plastic containers for intravenous injections | Current |
| BS EN ISO 3826-3:2007 | Plastics collapsible containers for human blood and blood components - Blood bag systems with integrated features | Current |
| BS EN ISO 3826-1:2003 | Plastics collapsible containers for human blood and blood components - Conventional containers | Current, Work in Hand |
| BS EN ISO 3826-2:2008 | Plastics collapsible containers for human blood and blood components - Graphical symbols for use on labels and instruction leaflets | Current |
| BS ISO 11663:2009 | Quality of dialysis fluid for haemodialysis and related therapies | Current, Work in Hand |
| BS ISO 6710:1995 | Single-use containers for venous blood specimen collection | Withdrawn |
| BS EN ISO 80369-1:2010 | Small bore connectors for liquids and gases in healthcare applications - General requirements | Current |
| BS 795:1983 | Specification for ampoules | Withdrawn |
| BS 4851:1982 | Specification for single use labelled medical specimen containers for haematology and biochemistry | Withdrawn |
| BS 4843:1987 | Specification for sterile intravascular cannula units for single use | Withdrawn |
| BS ISO 22413:2007 | Transfer sets for pharmaceutical preparations. Requirements and test methods | Withdrawn |
| BS EN ISO 22413:2011 | Transfer sets for pharmaceutical preparations. Requirements and test methods | Withdrawn |
| BS ISO 22413:2010 | Transfer sets for pharmaceutical preparations. Requirements and test methods | Withdrawn |
| BS EN ISO 22413:2013 | Transfer sets for pharmaceutical preparations. Requirements and test methods | Current |
| BS EN ISO 1135-4:2011 | Transfusion equipment for medical use - Transfusion sets for single use | Withdrawn |
| BS EN ISO 1135-4:2012 | Transfusion equipment for medical use - Transfusion sets for single use | Current |
| BS EN ISO 1135-4:2010 | Transfusion equipment for medical use - Transfusion sets for single use | Withdrawn |
| BS EN ISO 1135-4:2004 | Transfusion equipment for medical use - Transfusion sets for single use | Withdrawn |
| BS 2463-2:1989 | Transfusion equipment for medical use. - Specification for administration sets | Withdrawn |
| BS 2463-1:1990 | Transfusion equipment for medical use. - Specification for collapsible containers for blood and blood components | Withdrawn |
| BS ISO 13959:2009 | Water for haemodialysis and related therapies | Current, Work in Hand |
| BS ISO 26722:2009 | Water treatment equipment for haemodialysis applications and related therapies | Current, Work in Hand |