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AFNOR
NF P94-270
En Vigor
2020-10-30
Geotechnical design - Retaining structures - Reinforced and soil nailing structures
AFNOR
NF EN 300392-3-11
En Vigor
2025-01-22
Terrestrial Trunked Radio (TETRA) - Voice plus Data (V+D) - Part 3 :
interworking at the Inter-System Interface (ISI) - Sub-part 11 : general
design, SIP/IP (V1.2.1)
AFNOR
NF EN 4264
En Vigor
2020-02-26
Aerospace series - Heat resisting alloy X4NiCrMoTi43-13 - As forged -
Forging stock - a or D less than or equal to 200 mm
AFNOR
NF EN 17846
En Vigor
2023-11-01
Chemical disinfectants and antiseptics - Quantitative test method for
the evaluation of sporicidal activity against Clostridioides difficile
on non-porous surfaces with mechanical action employing wipes in the
medical area (4-field test) - Test method and requirements (phase 2,
step 2)
AFNOR
NF EN ISO 14907-1
En Vigor
2020-09-07
Electronic fee collection — Test procedures for user and fixed equipment
— Part 1: Description of test procedures
AFNOR
NF EN 1482-2
En Vigor
2024-12-18
Fertilizers, liming materials and inhibitors - Sampling and sample
preparation - Part 2 : general sample preparation provisions
AFNOR
NF ISO 18692-3
En Vigor
2020-08-15
Fibre ropes for offshore stationkeeping — Part 3: High modulus
polyethylene (HMPE)
AFNOR
NF EN 13048
En Vigor
2022-10-26
Packaging - Flexible aluminium tubes - Internal lacquer film thickness
measurement method
AFNOR
NF EN ISO 19443
En Vigor
2022-08-03
Quality management systems - Specific requirements for the application
of ISO 9001:2015 by organizations in the supply chain of the nuclear
energy sector supplying products and services important to nuclear
safety (ITNS)
AFNOR
NF EN 50367/A1
En Vigor
2022-10-07
Railway applications - Fixed installations and rolling stock - Criteria
to achieve technical compatibility between pantographs and overhead
contact line
AFNOR
NF EN 352-8/IN1
En Vigor
2024-04-03
Hearing protectors - Safety requirements - Part 8: Entertainment audio earmuffs
AFNOR
NF EN ISO 17664-1
En Vigor
2021-09-01
Processing of health care products - Information to be provided by the
medical device manufacturer for the processing of medical devices - Part
1 : critical and semi-critical medical devices










