Стандарт ÖNORM EN ISO 14971:2013-03

ÖNORM EN ISO 14971:2009-12

Заменен

Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)

DIN EN ISO 18113-5:2013-01

Действует

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2011 — 17 стр.

DIN EN ISO 18113-2:2013-01

Действует

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2011 — 19 стр.

DIN EN ISO 18113-5:2010-05

Отменен

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2009 — 18 стр.

DIN EN ISO 18113-3:2013-01

Действует

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011 — 18 стр.

DIN EN ISO 18113-4:2013-01

Действует

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009); German version EN ISO 18113-4:2011 — 20 стр.

DIN EN ISO 18113-1:2010-05

Отменен

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2009 — 62 стр.

DIN EN ISO 18113-3:2010-05

Отменен

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2009 — 19 стр.

DIN EN ISO 18113-2:2010-05

Отменен

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009); German version EN ISO 18113-2:2009 — 22 стр.

DIN EN ISO 18113-4:2010-05

Отменен

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009); German version EN ISO 18113-4:2009 — 21 стр.

DIN EN ISO 18113-1:2013-01

Действует

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009); German version EN ISO 18113-1:2011 — 60 стр.

DIN EN ISO 11608-5:2013-01

Действует

Needle-based injection systems for medical use - Requirements and test methods - Part 5: Automated functions (ISO 11608-5:2012); German version EN ISO 11608-5:2012 — 24 стр.

DIN EN ISO 14630:2009-08

Отменен

Non-active surgical implants - General requirements (ISO 14630:2008); German version EN ISO 14630:2009 — 25 стр.

DIN EN ISO 14630:2013-03

Действует

Non-active surgical implants - General requirements (ISO 14630:2012); German version EN ISO 14630:2012 — 23 стр.

DIN EN ISO 15223-1:2012-10

Отменен

Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2012); German version EN ISO 15223-1:2012, with CD-ROM — 43 стр.

ÖNORM EN 1789:2010-10

Заменен

Medical vehicles and their equipment - Road ambulances

ÖNORM EN 1865-2:2010-10

Заменен

Patient handling equipment used in road ambulances - Part 2: Power assisted stretcher

ÖNORM EN 1865-3:2012-07

Заменен

Patient handling equipment used in road ambulances - Part 3: Heavy duty stretcher

ÖNORM EN 1865-1:2010-10

Заменен

Patient handling equipment used in road ambulances - Part 1: General stretcher systems and patient handling equipment

ÖNORM EN ISO 11197:2009-09

Заменен

Medical supply units (ISO 11197:2004)

ÖNORM EN 455-3:2007-03

Заменен

Medical gloves for single use - Part 3: Requirements and testing for biological evaluation

ÖNORM EN 13718-1:2008-11

Заменен

Medical vehicles and their equipment - Air ambulances - Part 1: Requirements of medical devices used in air ambulances

ÖNORM EN 15908:2010-11

Заменен

Anaesthetic and respiratory equipment - Non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases

ÖNORM EN 13544-1:2010-02

Заменен

Respiratory therapy equipment - Part 1: Nebulizing systems and their components

ONR CEN/TR 16386:2013-07

Действует

Dentistry - Guidelines for handling methacrylate-based materials in the dental laboratory (CEN/TR 16386:2013)

ÖNORM EN 12182:2012-06

Действует

Assistive products for persons with disability - General requirements and test methods

ÖNORM EN 14931:2006-08

Действует

Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety requirements and testing

ÖNORM CEN/TS 15277:2006-12

Действует

Non-active surgical implants - Injectable implants

ÖNORM EN 1642:2012-02

Действует

Dentistry - Medical devices for dentistry - Dental implants

ÖNORM EN 1639:2010-03

Действует

Dentistry - Medical devices for dentistry - Instruments

ÖNORM EN 1640:2010-03

Действует

Dentistry - Medical devices for dentistry - Equipment