ISO 3826-2:2008
|
Plastics collapsible containers for human blood and blood components — Part 2: Graphical symbols for use on labels and instruction leaflets
|
ISO 10993-4:2017
|
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood
|
DIN EN ISO 15223-1:2015-08 (Draft)
|
MEDICAL DEVICES - SYMBOLS TO BE USED WITH MEDICAL DEVICE LABELS, LABELLING AND INFORMATION TO BE SUPPLIED - PART 1: GENERAL REQUIREMENTS (ISO 15223-1:2016, CORRECTED VERSION 2017-03)
|
DIN EN ISO 1135-4:2016-06
|
TRANSFUSION EQUIPMENT FOR MEDICAL USE - PART 4: TRANSFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 1135-4:2015)
|
DIN EN ISO 10993-11:2015-12 (Draft)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 11: TESTS FOR SYSTEMIC TOXICITY
|
ISO 3826-3:2006
|
Plastics collapsible containers for human blood and blood components — Part 3: Blood bag systems with integrated features
|
DIN EN ISO 23908:2013-10
|
SHARPS INJURY PROTECTION - REQUIREMENTS AND TEST METHODS - SHARPS PROTECTION FEATURES FOR SINGLE-USE HYPODERMIC NEEDLES, INTRODUCERS FOR CATHETERS AND NEEDLES USED FOR BLOOD SAMPLING (ISO 23908:2011)
|
DIN EN ISO 8536-4:2013-07
|
INFUSION EQUIPMENT FOR MEDICAL USE - PART 4: INFUSION SETS FOR SINGLE USE, GRAVITY FEED (ISO 8536-4:2010 + AMD 1:2013)
|
ISO 3826-1:2013
|
Plastics collapsible containers for human blood and blood components Part 1: Conventional containers
|
DIN EN ISO 10993-5:2009-10
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 5: TESTS FOR IN VITRO CYTOTOXICITY
|
ISO 10993-10:2010
|
Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization
|
ISO 10993-11:2017
|
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity
|
DIN EN ISO 10993-12:2012-10
|
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)
|
ISO 10993-12:2012
|
Biological evaluation of medical devices Part 12: Sample preparation and reference materials
|
DIN EN ISO 10993-4:2016-02 (Draft)
|
BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 4: SELECTION OF TESTS FOR INTERACTIONS WITH BLOOD (ISO 10993-4:2017)
|
DIN EN ISO 3826-3:2008-03
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 3: BLOOD BAG SYSTEMS WITH INTEGRATED FEATURES
|
DIN EN ISO 3826-1:2013-09
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 1: CONVENTIONAL CONTAINERS (ISO 3826-1:2013)
|
ISO 8536-4:2010
|
Infusion equipment for medical use Part 4: Infusion sets for single use, gravity feed
|
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
|
ISO 1135-4:2015
|
Transfusion equipment for medical use — Part 4: Transfusion sets for single use, gravity feed
|
DIN EN ISO 3826-2:2008-11
|
PLASTICS COLLAPSIBLE CONTAINERS FOR HUMAN BLOOD AND BLOOD COMPONENTS - PART 2: GRAPHICAL SYMBOLS FOR USE ON LABELS AND INSTRUCTION LEAFLETS
|
DIN EN ISO 10993-10:2014-10
|
Biological evaluation of medical devices - Part 10: Tests for irritation and skin sensitization (ISO 10993-10:2010)
|
ISO 3696:1987
|
Water for analytical laboratory use — Specification and test methods
|
ISO 23908:2011
|
Sharps injury protection Requirements and test methods Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling
|
ISO 594-2:1998
|
Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 2: Lock fittings
|
ISO 15223-1:2016
|
Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements
|
DIN ISO 3696:1991-06
|
WATER FOR ANALYTICAL LABORATORY USE - SPECIFICATION AND TEST METHODS
|
ISO 15747:2010
|
Plastic containers for intravenous injections
|