DIN EN ISO 13958:2016-03
|
CONCENTRATES FOR HAEMODIALYSIS AND RELATED THERAPIES (ISO 13958:2014)
|
DIN 13273-7:2003-08
|
CATHETER FOR MEDICAL USE - PART 7: DETERMINATION OF THE X-RAY ATTENUATION OF CATHETERS - REQUIREMENTS AND TESTING
|
DIN EN ISO 13959:2016-03
|
WATER FOR HAEMODIALYSIS AND RELATED THERAPIES (ISO 13959:2014)
|
DIN EN 13868:2002-11
|
Catheters - Test methods for kinking of single lumen catheters and medical tubing; German version EN 13868:2002
|
DIN 13273-8:2012-09
|
CATHETER FOR MEDICAL USE - PART 8: EPIDURAL CATHETERS
|
DIN EN ISO 26722:2016-02
|
WATER TREATMENT EQUIPMENT FOR HAEMODIALYSIS APPLICATIONS AND RELATED THERAPIES (ISO 26722:2014)
|
DIN EN ISO 10555-4:2013-11
|
Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2013)
|
DIN EN 1617:1997-04
|
STERILE DRAINAGE CATHETERS AND ACCESSORY DEVICES FOR SINGLE USE
|
DIN EN 455-4:2009-10
|
MEDICAL GLOVES FOR SINGLE USE - PART 4: REQUIREMENTS AND TESTING FOR SHELF LIFE DETERMINATION
|
DIN EN ISO 21171:2006-08
|
Medical gloves - Determination of removable surface powder (ISO 21171:2006)
|
DIN EN ISO 8637:2014-03
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - HAEMODIALYSERS, HAEMODIAFILTERS, HAEMOFILTERS AND HAEMOCONCENTRATORS (ISO 8637:2010, INCLUDING AMENDMENT 1:2013-04-01)
|
DIN EN ISO 4074:2016-05
|
NATURAL RUBBER LATEX MALE CONDOMS - REQUIREMENTS AND TEST METHODS (ISO 4074:2015)
|
DIN EN 455-3:2015-07
|
Medical gloves for single use - Part 3: Requirements and testing for biological evaluation
|
DIN EN ISO 11663:2016-02
|
QUALITY OF DIALYSIS FLUID FOR HAEMODIALYSIS AND RELATED THERAPIES (ISO 11663:2014)
|
DIN EN ISO 8670-2:1997-04
|
OSTOMY COLLECTION BAGS - PART 2: REQUIREMENTS AND TEST METHODS
|
DIN EN ISO 11070:2015-03
|
STERILE SINGLE-USE INTRAVASCULAR INTRODUCERS, DILATORS AND GUIDEWIRES (ISO 11070:2014)
|
DIN EN 1615:2001-01
|
ENTERAL FEEDING CATHETERS AND GIVING SETS FOR SINGLE USE AND THEIR CONNECTORS - DESIGN AND TESTING
|
DIN EN ISO 8669-2:1997-04
|
URINE COLLECTION BAGS - PART 2: REQUIREMENTS AND TEST METHODS
|
DIN 13222:2015-03
|
Absorption capacity of absorbent incontinence aids until leakage - Test method for measuring the suction capacity by use of a test torso
|
DIN EN 455-2:2015-07
|
Medical gloves for single use - Part 2: Requirements and testing for physical properties
|
DIN EN ISO 8638:2014-03
|
CARDIOVASCULAR IMPLANTS AND EXTRACORPOREAL SYSTEMS - EXTRACORPOREAL BLOOD CIRCUIT FOR HAEMODIALYSERS, HAEMODIAFILTERS AND HAEMOFILTERS (ISO 8638:2010)
|
DIN EN ISO 16021:2001-02
|
Urine absorbing aids - Basic principles for evaluation of single-use adult-incontinence-absorbing aids from the perspective of users and caregivers (ISO 16021:2000); German version EN ISO 16021:2000
|
DIN EN 1616:1999-05
|
STERILE URETHRAL CATHETERS FOR SINGLE USE
|
DIN EN 12439:1998-12
|
Sterile rectal catheters for single use; German version EN 12439:1998
|
DIN EN ISO 8836:2015-02
|
Suction catheters for use in the respiratory tract (ISO 8836:2014); German version EN ISO 8836:2014
|
DIN EN ISO 10555-1:2013-11
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 1: GENERAL REQUIREMENTS (ISO 10555-1:2013 + AMD 1:2017)
|
DIN EN 1618:1997-04
|
CATHETERS OTHER THAN INTRAVASCULAR CATHETERS - TEST METHODS FOR COMMON PROPERTIES
|
DIN EN ISO 10555-5:2013-11
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 5: OVER-NEEDLE PERIPHERAL CATHETERS (ISO 10555-5:2013)
|
DIN EN ISO 10555-3:2013-11
|
INTRAVASCULAR CATHETERS - STERILE AND SINGLE-USE CATHETERS - PART 3: CENTRAL VENOUS CATHETERS (ISO 10555-3:2013)
|
DIN EN ISO 7199:2015-06 (Draft)
|
CARDIOVASCULAR IMPLANTS AND ARTIFICIAL ORGANS - BLOOD-GAS EXCHANGERS (OXYGENATORS) (ISO 7199:2016)
|