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Transfusion, infusion & injection equipment

Standards in development (126)

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Standard TitleStatus
BS EN 50637 Medical electrical equipment - Particular requirements for the basic safety and essential performance of medical beds for childrenAccepted
BS EN 60370 Ed 2.0 Test procedure for thermal endurance of insulating resins and varnishes for impregnation purposes - Electric breakdown methodsPublic Comment
BS EN 60601-2-10 Ed2 A1 Medical electrical equipment Part 2-10: Particular requirements for the basic safety and essential performance of nerve and muscle stimulatorsApproval
BS EN 60601-2-16 Ed 5.0 Medical electrical equipment Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis; haemodiafiltration and haemofiltration equipmentAccepted
BS EN 60601-2-19 Ed.2 A1 Medical electrical equipment Part 2-19: Particular requirements for the basic safety and essential performance of infant incubatorsApproval
BS EN 60601-2-2 Ed 6.0 Medical electrical equipment Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessoriesPublic Comment
BS EN 60601-2-20 Ed.2 A1 Medical electrical equipment Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubatorsApproval
BS EN 60601-2-21 Ed.2 A1 Medical electrical equipment Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmersApproval
BS EN 60601-2-3 Ed.3 A1 Medical electrical equipment Part 2-3: Particular requirements for the basic safety and essential performance of short-wave therapy equipmentApproval
BS EN 60601-2-39 Ed 3.0 Medical electrical equipment Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipmentAccepted
BS EN 60601-2-40 Medical electrical equipment Part 2-40: Particular requirements for basic safety and essential performance of electromyographs and evoked response equipmentPublic Comment
BS EN 60601-2-46 Medical electrical equipment Part 2-46: Particular requirements for the basic safety and essential performance of operating tablesApproval
BS EN 60601-2-49 Ed 3.0 Medical electrical equipment Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment - Proposed Horizontal StandardPublic Comment
BS EN 60601-2-50:2009/A1 Medical electrical equipment Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipmentApproval
BS EN 60601-2-6 Ed.2 A1 Medical electrical equipment Part 2-6: Particular requirements for the basic safety and essential performance of microwave therapy equipmentApproval
BS EN 60601-2-75 Medical Electrical Equipment Part 2-75: Particular requirements for the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipmentAccepted
BS EN 60674-2 Ed 2.0 IEC 60674-2/Ed2: Specification for plastic films for electrical purposes. Part 2: Methods of testApproval
BS EN 60674-3-8 Ed 1.0 /A1 Amendment 1: Plastic films for electrical purposes -Part 3: Specifications for individual materials - Sheet 8: Balanced biaxially oriented polyethylene naphthalate (PEN) films used for electrical insulationApproval
BS EN 60893-3-6 Ed 2.0 /A2 Amendment 2: Insulating materials - Industrial rigid laminated sheets based on thermosetting resins for electrical purposes Part 3-6: Specifications for individual materials - Requirements for rigid laminated sheets based on silicone resinsAccepted
BS EN 62677-3-103 Heat-shrinkable low and medium voltage moulded shapes Part 3: Material requirements - Sheet 103: Heat-shrinkable; polyolefin; semi-conductive moulded shapes for medium voltage applicationsAccepted
BS EN 80601-2-35 Ed.2 A1 Medical electrical equipment Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical useApproval
BS EN 80601-2-58:2015/A1 Medical electrical equipment Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgeryPublic Comment
BS EN 80601-2-60 Medical electrical equipment Part 2-60: Particular requirements for the basic safety and essential performance of dental equipment NULLAccepted
BS EN 80601-2-71 Medical electrical equipment Part 2-71: Particular requirements for basic safety and essential performance of functional near-infrared spectroscopy (NIRS) equipmentPublication
BS EN ISO 18559 Dentistry - Spatulas for dental materialsPublic Comment
BS ENISO 10555-1:2013 Amd 1 Sterile and single-use catheters Intravascular catheters — Sterile and single-use catheters - Part 1: General requirements - Amendment 1Public Comment
BS ENISO 10650 Amd 1 activators – Amendment 1Accepted
BS ENISO 1135-3 Transfusion equipment for medical use Part 3: Blood-taking setApproval
BS ENISO 11608-4 Pen-injectors for medical use Part 4: Requirements and test methods for electronic and electromechanical pen-injectorsPublic Comment
BS ENISO 11608-7 Needle-based injection devices for visually-impaired patientsApproval
BS ENISO 13666 Ophthalmic optics - Spectacle lenses - VocabularyAccepted
BS ENISO 13897 Dentistry -- Amalgam capsulesAccepted
Opens a new windowBS ENISO 14457 Dentistry - Handpieces and motorsPublic Comment
BS ENISO 14708-3 implantable medical devices Part 3: Implantable neurostimulatorsPublic Comment
BS ENISO 17509 Dentistry - Torque transmitter for handpiecesApproval
BS ENISO 1797 Dentistry - Shanks for rotary, oscillating and reciprocating instrumentsPublic Comment
BS ENISO 19490 Dentistry - Sinus elevatorPublic Comment
BS ENISO 19715 Dentistry - Filling instruments with contra setPublic Comment
BS ENISO 20166-1 examinations Specifications for pre-examination processes for FFPE tissue - RNAPublic Comment
BS ENISO 20166-2 examinations - Specifications for pre-examination processes for FFPE tissue Part 2: Isolated proteinsPublic Comment
BS ENISO 20166-3 examinations - Specifications for pre-examination processes for FFPE tissue Part 3: Isolated DNAPublic Comment
BS ENISO 20184-1 examinations - Specifications for pre-examination processes for frozen tissue - RNAPublic Comment
BS ENISO 20184-2 examinations - Specifications for pre-examination processes for frozen tissue Part 2: Isolated proteinsPublic Comment
BS ENISO 20186-1 examinations - Specifications for pre-examination processes for blood - Cellular RNAAccepted
BS ENISO 20186-2 examinations - Specifications for pre-examination processes for blood - Cellular RNA Part 2: Isolated genomic DNA correctAccepted
BS ENISO 20186-3 examinations - Specifications for pre-examination processes for blood - Cellular RNA Part 3: Isolated circulating cell free DNA from plasmaAccepted
BS ENISO 20695 Enteral feeding catheters and enteral giving sets for single use andtheir connectorsAccepted
BS ENISO 20696 Sterile urethal catheters for single useAccepted
BS ENISO 20697 Sterile drainage catheters and accessory devices for single useAccepted
BS ENISO 21987 Ophthalmic optics - Mounted spectacle lensesPublic Comment
BS ENISO 22870 Requirements for quality and competenceApproval
BS ENISO 25539-1 Cardiovascular implants - Endovascular devices Part 1: Endovascular prosthesesPublic Comment
BS ENISO 3964 Dentistry - Coupling dimensions for handpiecesApproval
BS ENISO 5364 Oropharyngeal airwaysApproval
BS ENISO 5366-1 Anaesthetic and respiratory equipment - Tracheostomy tubes Part : Tubes and connectors for use in adultsApproval
BS ENISO 6009 Hypodermic needles for single use - Colour coding for identificationPublication
BS ENISO 7198 Cardiovascular implants - Tubular vascular prosthesesApproval
BS ENISO 7199 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)Public Comment
BS ENISO 7488 Dental amalgamatorsAccepted
BS ENISO 7492 Dental explorersAccepted
BS ENISO 7787-3 Dental rotary instruments - Cutters Part 3: Carbide laboratory cutters for milling machinesPublic Comment
BS ENISO 7864 Sterile hypodermic needles for single useApproval
BS ENISO 7886-1 Sterile hypodermic syringes for single use Part 1: Syringes for manual usePublic Comment
BS ENISO 7886-3 Sterile hypodermic syringes for single use Part 3: Auto-disable syringes for fixed-dose immunizationAccepted
BS ENISO 80369-1 gases in healthcare applications Part 1: General requirementsPublic Comment
BS ENISO 80369-3 liquids and gases in healthcare applications Part 3: Connectors for enteral applicationsPublication
BS ENISO 80369-7 Small bore connectors for liquids and gases in healthcare applications Part 7: Connectors with 6% (Luer) taper for intravascular or hypodermic applicationsApproval
BS ENISO 8536-13 Infusion equipment for medical use Part 13: Clamps, restrictors and flow regulators for transfusion and infusion setsApproval
BS ENISO 8536-14 Infusion equipment for medical use Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contactApproval
Opens a new windowBS ENISO 8637-1 Extracorporeal systems for blood purification Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentratorsPublic Comment
Opens a new windowBS ENISO 8637-2 Extracorporeal systems for blood purification Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofiltersPublic Comment
BS ENISO 8871-5 Elastomeric parts for parenterals and for devices for pharmaceutical use Part 5: Functional requirements and testingApproval
BS ENISO 8980-1 Ophthalmic optics - Uncut finished spectacle lenses Part 1: Specifications for single-vision and multifocal lensesPublic Comment
BS ENISO 8980-2 Ophthalmic optics - Uncut finished spectacle lenses Part 2: Specifications for continuous variation power lenses, including progressive power lensesPublic Comment
BS ENISO 9173-1 Dentistry - Extraction forceps Part 1: General requirements and test methodsApproval
BS ENISO 9626 manufacture of medical devicesPublication
BS ENISO 9687:2015 Amd 1 for dental equipment - Amendment 1Accepted
BS ENISO 9873 Dental hand instruments - Reusable mirrors and handlesPublic Comment
BS IEC 80369-5 liquids and gases in healthcare applications Part 5: Connectors for limb cuff inflation applicationsPublication
BS IEC 80601-2-30 Medical electrical equipment Part 2-30: Particular requirements for basic safety and essential performance of automated non-invasive sphygmomanometersPublic Comment
BS ISO 4957 Tool steelsIdea
BS ISO 10637 Dentistry - High and medium volume suction systems for dental equipmentIdea
BS ISO 11040-8 Prefilled syringes Part 8: Requirements and test methods for the use of filled syringesApproval
BS ISO 11418-1 Containers and accessories for pharmaceutical preparations Part 1: Drop-dispensing glass bottlesPublic Comment
BS ISO 11418-2 Containers and accessories for pharmaceutical preparations Part 2: Screw-neck glass bottles for syrupsPublic Comment
BS ISO 11418-3 Containers and accessories for pharmaceutical preparations Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage formsPublic Comment
BS ISO 11418-7 Containers and accessories for pharmaceutical preparations Part 7: Screw-neck vials made of glass tubing for liquid dosage formsPublication
Opens a new windowBS ISO 11608-6 Needle-based injection systems for medical use - Requirements and test methods Part 6: Bolus InjectorsPublic Comment
BS ISO 15195 Laboratory medicine - Requirements for the competence of calibration laboratories using reference measurement proceduresAccepted
BS ISO 15674 Cardiovascular implants and artificial organs - Hard-shell cardiotomy/venous reservoir systems (with/without filter) and soft venous reservoir bagsPublic Comment
BS ISO 15675 Cardiovascular implants and artificial organs - Cardiopulmonary bypass systems - Arterial blood line filtersPublic Comment
BS ISO 15676 Cardiovascular implants and artificial organs - Requirements for single-use tubing packs for cardiopulmonary bypass and extracorporeal membrane oxygenation (ECMO)Public Comment
BS ISO 16142-2 Medical devices - Recognized essential principles of safety and performance of medical devices Part 2: General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standardsPublic Comment
BS ISO 16782 Clinical laboratory testing - Criteria for acceptable lots of dehydrated Mueller-Hinton agar and broth for antimicrobial susceptibility testingPublication
BS ISO 18190 Anaesthetic and respiratory equipment - General requirements for airways and related equipmentApproval
BS ISO 18241 Cardiovascular implants and extracorporeal systems - Cardiopulmonary bypass systems - Venous bubble trapsPublic Comment
BS ISO 18242 Cardiovascular implants and extracorporeal systems - Centrifugal blood pumpsPublic Comment
BS ISO 18250-1 Connectors for reservoir delivery systems for healthcare applications Part 1: General requirementsAccepted
BS ISO 18250-3 Connectors for enteral feed/solution reservoirsPublic Comment
BS ISO 18250-8 Connectors for reservoir delivery systems for healthcare applications Part 8: Connectors for citrate-based anticoagulant solution for apheresis applicationsPublic Comment
BS ISO 19211 Automatic fire safety valves for use during oxygen therapyAccepted
BS ISO 20164 Molecular in-vitro diagnostic examinations Specifications for pre-examination processes for FFPE tissue DNAPublic Comment
BS ISO 20569 Dentistry - Trephine bursAccepted
BS ISO 20570 Dentistry - Oral surgical scalpel handleAccepted
BS ISO 20608 Dentistry - Powder jet handpiecesAccepted
BS ISO 21533 Dentistry - Reusable cartridge syringes intended for intraligamentary injectionsAccepted
BS ISO 23500-1 Guidance for the preparation and quality management of fluids for haemodialysis and related therapiesAccepted
BS ISO 23500-2 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies Part 2: Water treatment equipment for haemodialysis applications and related therapiesAccepted
BS ISO 23500-3 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies Part 3: Water for haemodialysis and related therapiesAccepted
BS ISO 23500-4 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies Part 4: Concentrates for haemodialysis and related therapiesAccepted
BS ISO 23500-5 Guidance for the preparation and quality management of fluids for haemodialysis and related therapies Part 5: Quality of dialysis fluid for haemodialysis and related therapiesAccepted
BS ISO 35001 Laboratory biorisk management system - RequirementsAccepted
BS ISO 3630-1 Dentistry - Endodontic instruments Part 1: General requirementsAccepted
BS ISO 4802-1 Glassware - Hydrolytic resistance of the interior surfaces of glass containers Part 1: Determination by titration method and classificationPublication
BS ISO 4802-2 Glassware - Hydrolytic resistance of the interior surfaces of glass containers Part 2: Determination by flame spectrometry and classificationPublication
BS ISO 5910 Cardiovascular implants and extracoporeal systems - Cardiac valve repair devicesAccepted
BS ISO 7494-1 Dentistry - Dental unit and patient chair Part 1: General requirements and test methodsAccepted
BS ISO 8536-6 Infusion equipment for medical use Part 6: Freeze drying closures for infusion bottlesPublic Comment
Opens a new windowBS ISO 8637-3 Extracorporeal systems for blood purification Part 3: Plasmafilters in order to join the new series on blood purificationPublic Comment
BSENENISO 5361 Tracheal tubes and connectorsApproval
PD CEN/TS 16945 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine, venous blood serum and plasmaPublication
PD IEC/TR 60893-4 Ed 2.0 /A1 AMENDMENT 1: Insulating materials - Industrial rigid laminated sheets based on thermosetting resins for electrical purposes Part 4: Typical valuesApproval
PD ISO/TR 12417-2 Cardiovascular implants and extracorporeal systems - Vascular device-drug combination products Part 2: Local regulatory guidanceAccepted
PD ISO/TR 19024 Evaluation of CPB devices relative to their capabilities of reducing the transmission of Gaseous MicroEmboli(GME)to a patient during cardiopulmonary bypassPublication
PD ISO/TR 19727 Medical devices - Pump tube spallation test - General procedureAccepted
PD ISO/TS 20658 Medical laboratory examinations - Requirements for collection, transport, receipt, and handling of samplesAccepted

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Published standards (110)

Sort by: Reference | Title | Status

Standard referenceNameStatus
BS EN ISO 8872:2003Aluminium caps for transfusion, infusion and injection bottles. General requirements and test methodsCurrent
BS EN 28872:1993Aluminium caps for transfusion, infusion and injection bottles. General requirements and test methodsWithdrawn
BS EN 1707:1997Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment. Lock fittingsCurrent
BS EN 20594-1:1994Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - General requirementsCurrent
BS 3930-2:1991Conical fittings with a 6% (Luer) taper for syringes, needles and other medical equipment - Specification for lock fittingsWithdrawn
BS ISO 11418-3:2005Containers and accessories for pharmaceutical preparations - Screw-neck glass bottles (veral) for solid and liquid dosage formsCurrent, Work in Hand
BS ISO 11418-5:2015Containers and accessories for pharmaceutical preparations - Dropper assembliesCurrent
BS ISO 11418-4:2005Containers and accessories for pharmaceutical preparations - Tablet glass bottlesCurrent
BS ISO 11418-1:2005Containers and accessories for pharmaceutical preparations - Drop-dispensing glass bottlesCurrent, Work in Hand
BS ISO 11418-2:2005Containers and accessories for pharmaceutical preparations - Screw-neck glass bottles for syrupsCurrent, Work in Hand
BS ISO 15010:1998Disposable hanging devices for transfusion and infusion bottles. Requirements and test methodsCurrent
BS EN ISO 8871:1997Elastomeric parts for aqueous parenteral preparationsWithdrawn
BS EN ISO 8871-5:2014Elastomeric parts for parenterals and for devices for pharmaceutical use - Functional requirements and testingCurrent, Work in Hand
BS EN ISO 8871-4:2006Elastomeric parts for parenterals and for devices for pharmaceutical use - Biological requirements and test methodsCurrent
BS EN ISO 8871-1:2004Elastomeric parts for parenterals and for devices for pharmaceutical use - Extractables in aqueous autoclavatesCurrent
BS EN ISO 8871-2:2004+A1:2014Elastomeric parts for parenterals and for devices for pharmaceutical use - Identification and characterizationCurrent
BS EN ISO 8871-3:2004Elastomeric parts for parenterals and for devices for pharmaceuticals use - Determination of released-particle countCurrent
BS EN ISO 23500:2015Guidance for the preparation and quality management of fluids for haemodialysis and related therapiesCurrent
BS ISO 23500:2011Guidance for the preparation and quality management of fluids for haemodialysis and related therapiesWithdrawn
BS EN 1283:1996Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuitsWithdrawn
BS ISO 15375:2004Hanging devices for multiple use with infusion bottles. Requirements and test methodsWithdrawn
BS EN ISO 8536-1:2008Infusion equipment for medical use - Infusion glass bottlesWithdrawn
BS EN ISO 8536-4:2007Infusion equipment for medical use - Infusion sets for single use, gravity feedWithdrawn
BS EN ISO 8536-4:2010Infusion equipment for medical use - Infusion sets for single use, gravity feedWithdrawn
BS EN ISO 8536-1:2011Infusion equipment for medical use - Infusion glass bottles Current
BS EN ISO 8536-1:1999Infusion equipment for medical use - Infusion glass bottlesWithdrawn
BS EN ISO 8536-10:2004Infusion equipment for medical use - Accessories for fluid lines for use with pressure infusion equipmentWithdrawn
BS EN ISO 8536-8:2004Infusion equipment for medical use - Infusion equipment for use with pressure infusion apparatusWithdrawn
BS EN ISO 8536-3:1999Infusion equipment for medical use - Aluminium caps for infusion bottlesWithdrawn
BS EN ISO 8536-2:1999Infusion equipment for medical use - Closures for infusion bottlesWithdrawn
BS EN ISO 8536-11:2004Infusion equipment for medical use - Infusion filters for use with pressure infusion equipmentWithdrawn
BS EN ISO 8536-9:2004Infusion equipment for medical use - Fluid lines for use with pressure infusion equipmentWithdrawn
BS EN ISO 8536-9:2015Infusion equipment for medical use - Fluid lines for single use with pressure infusion equipmentCurrent
BS EN ISO 8536-2:2010Infusion equipment for medical use - Closures for infusion bottlesCurrent
BS EN ISO 8536-3:2009Infusion equipment for medical use - Aluminium caps for infusion bottles Current
BS EN ISO 8536-4:2004Infusion equipment for medical use - Infusion sets for single use, gravity feedWithdrawn
BS EN ISO 8536-8:2015Infusion equipment for medical use - Infusion sets for single use with pressure infusion apparatusCurrent
BS EN ISO 8536-10:2015Infusion equipment for medical use - Accessories for fluid lines for single use with pressure infusion equipmentCurrent
BS EN ISO 8536-2:2002Infusion equipment for medical use - Closures for infusion bottlesWithdrawn
BS EN ISO 8536-5:2013Infusion equipment for medical use - Burette infusion sets for single use, gravity feedCurrent
BS EN ISO 8536-4:2013+A1:2013Infusion equipment for medical use - Infusion sets for single use, gravity feedCurrent
BS EN ISO 8536-5:2011Infusion equipment for medical use - Burette infusion sets for single use, gravity feedWithdrawn
BS EN ISO 8536-11:2015Infusion equipment for medical use - Infusion filters for single use with pressure infusion equipmentCurrent
BS ISO 8536-7:2009Infusion equipment for medical use - Caps made of aluminium-plastics combinations for infusion bottlesCurrent
BS EN ISO 8536-1:2003Infusion equipment for medical use - Infusion glass bottlesWithdrawn
BS ISO 8536-12:2007+A1:2013Infusion equipment for medical use - Check valvesCurrent
BS EN ISO 8362-2:2015Injection containers and accessories - Closures for injection vialsCurrent
BS EN ISO 8362-4:2011Injection containers and accessories - Injection vials made of moulded glassCurrent
BS EN ISO 8362-7:2010Injection containers and accessories - Injection caps made of aluminium-plastics combinations without overlapping plastics partCurrent
BS EN ISO 8362-6:2011Injection containers and accessories - Caps made of aluminium-plastics combinations for injection vialsCurrent
BS EN ISO 8362-3:2003Injection containers and accessories - Aluminium caps for injection vialsCurrent
BS EN ISO 8362-2:2010Injection containers and accessories - Closures for injection vialsWithdrawn
BS EN ISO 8362-1:2004Injection containers and accessories - Injection vials made of glass tubingWithdrawn
BS EN ISO 8362-5:2016Injection containers and accessories - Freeze drying closures for injection vialsCurrent
BS EN ISO 8362-1:2009+A1:2015Injection containers and accessories - Injection vials made of glass tubingCurrent
BS EN ISO 8362-4:2004Injection containers and accessories - Injection vials made of moulded glassWithdrawn
BS EN 28362-1:1993Injection containers for injectables and accessories - Injection vials made of glass tubingWithdrawn
BS EN 28362-3:1993Injection containers for injectables and accessories - Aluminium caps for injection vialsWithdrawn
BS EN 28362-2:1993Injection containers for injectables and accessories - Closures for injection vialsWithdrawn
BS EN 28362-4:1993Injection containers for injectables and accessories - Injection vials made of moulded glassWithdrawn
BS EN ISO 9187-1:2003Injection equipment for medical use - Ampoules for injectablesWithdrawn
BS EN ISO 9187-2:1999Injection equipment for medical use - One-point-cut (OPC) ampoulesWithdrawn
BS EN ISO 9187-1:1999Injection equipment for medical use - Ampoules for injectablesWithdrawn
BS EN ISO 9187-1:2008Injection equipment for medical use - Ampoules for injectablesWithdrawn
BS EN ISO 9187-1:2010Injection equipment for medical use - Ampoules for injectablesCurrent
BS EN ISO 9187-2:2010Injection equipment for medical use - One-point-cut (OPC) ampoulesCurrent
PD CR 13825:2000Luer connectors. A report to CEN CHeF from the CEN forum task group 'Luer fittings'Current
BS ISO 28620:2010Medical devices. Non-electrically driven portable infusion devicesCurrent
BS EN 60601-2-16:2015Medical electrical equipment - Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipmentCurrent
BS EN 60601-2-24:2015Medical electrical equipment - Particular requirements for the basic safety and essential performance of infusion pumps and controllersCurrent
BS EN 60601-2-39:1999Medical electrical equipment. Particular requirements for safety - Particular requirements for safety. Specification for peritoneal dialysis equipmentWithdrawn
BS EN 60601-2-24:1998Medical electrical equipment. Particular requirements for safety - Particular requirements for the safety of infusion pumps and controllersCurrent
BS EN 60601-2-16:1998Medical electrical equipment. Particular requirements for safety - Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipmentWithdrawn
BS EN 50072:1992Medical electrical equipment. Particular requirements for safety. Specification for peritoneal dialysis equipmentWithdrawn
PD IEC/PAS 63023:2016Medical electrical system. Input interface for haemodialysis equipment for use of external alarming deviceCurrent
BS ISO 15375:2010Medical infusion bottles. Suspension devices for multiple use. Requirements and test methodsCurrent
BS EN ISO 21649:2009Needle-free injectors for medical use. Requirements and test methodsCurrent
BS EN ISO 21649:2006Needle-free injectors for medical use. Requirements and test methodsWithdrawn
BS EN ISO 15747:2005Plastic containers for intravenous injectionWithdrawn
BS EN ISO 15747:2010Plastic containers for intravenous injectionsWithdrawn
BS EN ISO 15747:2011Plastic containers for intravenous injectionsCurrent
BS EN ISO 3826-1:2003Plastics collapsible containers for human blood and blood components - Conventional containersWithdrawn
BS EN ISO 3826-3:2007Plastics collapsible containers for human blood and blood components - Blood bag systems with integrated featuresCurrent
BS EN ISO 3826-4:2015Plastics collapsible containers for human blood and blood components - Aphaeresis blood bag systems with integrated featuresCurrent
BS EN ISO 3826-2:2008Plastics collapsible containers for human blood and blood components - Graphical symbols for use on labels and instruction leafletsCurrent
BS EN ISO 3826-1:2013Plastics collapsible containers for human blood and blood components - Conventional containersCurrent
BS EN ISO 11663:2015Quality of dialysis fluid for haemodialysis and related therapiesCurrent
BS ISO 11663:2009Quality of dialysis fluid for haemodialysis and related therapiesWithdrawn
BS ISO 6710:1995Single-use containers for venous blood specimen collectionWithdrawn
BS EN ISO 80369-1:2010Small bore connectors for liquids and gases in healthcare applications - General requirementsCurrent, Work in Hand
BS 795:1983Specification for ampoulesWithdrawn
BS 4851:1982Specification for single use labelled medical specimen containers for haematology and biochemistryWithdrawn
BS 4843:1987Specification for sterile intravascular cannula units for single useWithdrawn
BS EN ISO 8537:2016Sterile single-use syringes, with or without needle, for insulinCurrent
BS ISO 22413:2007Transfer sets for pharmaceutical preparations. Requirements and test methodsWithdrawn
BS EN ISO 22413:2013Transfer sets for pharmaceutical preparations. Requirements and test methodsCurrent
BS ISO 22413:2010Transfer sets for pharmaceutical preparations. Requirements and test methodsWithdrawn
BS EN ISO 22413:2011Transfer sets for pharmaceutical preparations. Requirements and test methodsWithdrawn
BS EN ISO 1135-4:2011Transfusion equipment for medical use - Transfusion sets for single useWithdrawn
BS EN ISO 1135-4:2010Transfusion equipment for medical use - Transfusion sets for single useWithdrawn
BS EN ISO 1135-4:2015Transfusion equipment for medical use - Transfusion sets for single use, gravity feedCurrent
BS EN ISO 1135-4:2012Transfusion equipment for medical use - Transfusion sets for single use Withdrawn
BS EN ISO 1135-5:2015Transfusion equipment for medical use - Transfusion sets for single use with pressure infusion apparatusCurrent
BS EN ISO 1135-4:2004Transfusion equipment for medical use - Transfusion sets for single useWithdrawn
BS 2463-2:1989Transfusion equipment for medical use - Specification for administration setsWithdrawn
BS 2463-1:1990Transfusion equipment for medical use - Specification for collapsible containers for blood and blood componentsWithdrawn
BS EN ISO 13959:2015Water for haemodialysis and related therapiesCurrent
BS ISO 13959:2009Water for haemodialysis and related therapiesWithdrawn
BS EN ISO 26722:2015Water treatment equipment for haemodialysis applications and related therapiesCurrent
BS ISO 26722:2009Water treatment equipment for haemodialysis applications and related therapiesWithdrawn

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