EN 28601 : 1992
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
DATA ELEMENTS AND INTERCHANGE FORMATS - INFORMATION INTERCHANGE - REPRESENTATION OF DATES AND TIMES
11-12-2004
01-12-2013
National foreword
Committees responsible
Specification
0. Introduction
1. Scope and field of application
2. References
3. Terms and definitions
4. Fundamental principles
5. Representations
Annexes
A. Relationship to ISO 2014, 2015, 2711, 3307 and 4031
B. Examples of representation of dates, time of the day,
combinations of data and time, and periods of time
Explains the representation of dates in the Gregorian calender including calendar dates expressed in terms of year, month and day of month; ordinal dates expressed in terms of year and day of year; dates identified by means of year, week numbers and day numbers; time of the day based upon the 24-hour timekeeping system; differences between local time and Coordinated Universal Time, combination of date and time and periods of time, with or without either a start or end date or both.
Committee |
CEN/CS F17
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Withdrawn
|
Standards | Relationship |
NS ISO 8601 : 3ED 2006 | Identical |
PN EN 28601 : 2002 | Identical |
NBN EN 28601 : 1993 | Identical |
BS EN 28601:1992 | Identical |
SN EN 28601 : 1994 | Identical |
NF EN 28601 : 1993 | Identical |
UNI EN 28601 : 1993 | Identical |
UNE-EN 28601:1995 | Identical |
ISO 8601:2004 | Identical |
NEN ISO 8601 : 2005 | Identical |
I.S. EN 28601:1993 | Identical |
DIN EN 28601:1993-02 | Identical |
DD ENV 13376:1999 | Geographic information. Data description. Rules for application schemas |
03/108542 DC : DRAFT MAY 2003 | BS EN ISO 11140-1 - STERILIZATION OF HEALTH CARE PRODUCTS - CHEMICAL INDICATORS - PART 1: GENERAL REQUIREMENTS |
11/30238497 DC : 0 | BS EN 13160-5 - LEAK DETECTION SYSTEMS - PART 5: TANK GAUGE LEAK DETECTION SYSTEMS |
DD ENV 12018:1998 | Identification, administrative, and common clinical data structure for intermittently connected devices used in healthcare (including machine readable cards) |
08/30184612 DC : DRAFT SEP 2008 | BS EN 1641 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
PD CR 1750:1999 | Identification card systems. Inter-sector messages between devices and hosts. Acceptor to acquirer messages |
CEI EN 62298-3 : 2005 | TELEWEB APPLICATION - PART 3: SUPERTELETEXT PROFILE |
02/563808 DC : DRAFT SEP 2002 | BS EN 1639 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
02/563845 DC : DRAFT SEP 2002 | BS EN 1642 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - DENTAL IMPLANTS |
BS EN 375:2001 | Information supplied by the manufacturer with in vitro diagnostic reagents for professional use |
EN 12381:2005 | Health informatics - Time standards for healthcare specific problems |
EN 61313-1:1997 | Fibre optic passive components and cable assemblies - Part 1: Capability approval - Generic specification |
I.S. EN 592:2002 | INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING |
07/30167327 DC : DRAFT AUG 2007 | BS EN 868-7 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 7: ADHESIVE COATED PAPER FOR THE MANUFACTURE OF SEALABLE PACKS FOR MEDICAL USE FOR STERILIZATION BY ETHYLENE OXIDE OR IRRADIATION - REQUIREMENTS AND TEST METHODS |
I.S. EN ISO 1567:2000 | DENTISTRY - DENTURE BASE POLYMERS |
07/30166924 DC : DRAFT AUG 2007 | BS EN 868-2 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 2: STERILIZATION WRAP - REQUIREMENTS AND TEST METHODS |
02/653358 DC : DRAFT NOV 2002 | ISO/DIS 21549-2 - HEALTH INFORMATICS - PATIENT HEALTHCARE DATA - PART 2: COMMON OBJECTS |
02/563832 DC : DRAFT SEP 2002 | BS EN 1641 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - MATERIALS |
BS EN 62298-3:2005 | Teleweb application Superteletext profile |
BS EN 45502-2-1:2003 | Active implantable medical devices Particular requirements for active implantable medical devices intended to treat bradyarrhythmia (cardiac pacemakers) |
I.S. EN 45502-2-2:2008 | ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-2: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT TACHYARRHYTHMIA (INCLUDES IMPLANTABLE DEFIBRILLATORS) |
I.S. ENV 13376:1999 | GEOGRAPHIC INFORMATION - DATA DESCRIPTION - RULES FOR APPLICATION SCHEMES |
I.S. EN 62298-3:2005 | TELEWEB APPLICATION - PART 3: SUPERTELETEXT PROFILE |
I.S. EN ISO 14727:1999 | DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE |
EN 45502-2-2 : 2008 COR 2009 | ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-2: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT TACHYARRHYTHMIA (INCLUDES IMPLANTABLE DEFIBRILLATORS) |
08/30191609 DC : DRAFT DEC 2008 | BS ISO 14708-6 - IMPLANTS FOR SURGERY - ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 6: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT TACHYARRHYTHMIA (INCLUDING IMPLANTABLE DEFIBRILLATORS) |
08/30184602 DC : DRAFT SEP 2008 | BS EN 1639 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS |
DD ENV 1613:1996 | Medical informatics. Messages for exchange of laboratory information |
I.S. EN 376:2002 | INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
CEI EN 62099 : 2002 | FIBRE OPTIC WAVELENGTH SWITCHES - GENERIC SPECIFICATION |
DD ENV 12656:1999 | Geographic information. Data description. Quality |
BS EN 45502-2-2:2008 | Active implantable medical devices Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (includes implantable defibrillators) |
07/30166933 DC : DRAFT AUG 2007 | BS EN 868-5 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 5: SEALABLE POUCHES AND REELS OF POROUS MATERIALS AND PLASTIC FILM CONSTRUCTION - REQUIREMENTS AND TEST METHODS |
PREN 13160-5 : DRAFT 2014 | LEAK DETECTION SYSTEMS - PART 5: REQUIREMENTS AND TEST/ASSESSMENT METHODS FOR IN-TANK GAUGE SYSTEMS AND PRESSURISED PIPEWORK SYSTEMS |
ES 201 208 : 1.2.1 | IDENTIFICATION CARD SYSTEMS; TELECOMMUNICATIONS IC CARDS AND TERMINALS; ADDITIONAL TELECOMMUNICATIONS FEATURES (ATF) |
BS EN 12381:2005 | Health informatics. Time standards for healthcare specific problems |
BS EN ISO 2566-2:2001 | Steel. Conversion of elongation values Austenitic steels |
I.S. EN 12381:2005 | HEALTH INFORMATICS - TIME STANDARDS FOR HEALTHCARE SPECIFIC PROBLEMS |
ENV 12018 : DRAFT 1997 | IDENTIFICATION, ADMINISTRATIVE, AND COMMON CLINICAL DATA STRUCTURE FOR INTERMITTENTLY CONNECTED DEVICES USED IN HEALTHCARE (INCLUDING MACHINE READABLE CARDS) |
ENV 12661 : DRAFT 1998 | GEOGRAPHIC INFORMATION - REFERENCING - GEOGRAPHIC IDENTIFIERS |
ENV 12657 : DRAFT 1998 | GEOGRAPHIC INFORMATION - DATA DESCRIPTION - METADATA |
ENV 12656 : DRAFT 1998 | GEOGRAPHIC INFORMATION - DATA DESCRIPTION - QUALITY |
DD ENV 12661:1999 | Geographic information. Referencing. Geographic identifiers |
02/563809 DC : DRAFT SEP 2002 | BS EN 980 - GRAPHICAL SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
BS ISO 7886-2 : 1996 AMD 9835 | STERILE HYPODERMIC SYRINGES FOR SINGLE USE - SYRINGES FOR USE WITH POWER-DRIVEN SYRINGE PUMPS |
DD ENV 12657:1999 | Geographic information. Data description. Metadata |
14/30301263 DC : 0 | BS EN 13160-5 - LEAK DETECTION SYSTEMS - PART 5: REQUIREMENTS AND TEST/ASSESSMENT METHODS FOR IN-TANK GAUGE SYSTEMS AND PRESSURISED PIPEWORK SYSTEMS |
07/30166930 DC : DRAFT AUG 2007 | BS EN 868-4 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 4: PAPER BAGS - REQUIREMENTS AND TEST METHODS |
07/30166936 DC : DRAFT AUG 2007 | BS EN 868-6 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 6: PAPER FOR THE MANUFACTURE OF STERILE BARRIER SYSTEMS INTENDED FOR STERILIZATION BY LOW TEMPERATURE STERILIZATION PROCESSES OR IRRADIATION - REQUIREMENTS AND TEST METHODS |
11/30247124 DC : 0 | BS EN ISO 14819-1 - INTELLIGENT TRANSPORT SYSTEMS - TRAFFIC AND TRAVEL INFORMATION MESSAGES VIA TRAFFIC MESSAGE CODING - PART 1: CODING PROTOCOL FOR RADIO DATA SYSTEM - TRAFFIC MESSAGE CHANNEL (RDS-TMC) USING ALERT-C |
02/563818 DC : DRAFT SEP 2002 | BS EN 1640 - DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - EQUIPMENT |
BS EN 61747-1:2000 | Liquid crystal and solid-state display devices Generic specification |
CEI EN 61313-1 : 1998 | FIBRE OPTIC PASSIVE COMPONENTS AND CABLE ASSEMBLIES - PART 1: CAPABILITY APPROVAL - GENERIC SPECIFICATION |
I.S. EN 45502-2-1:2004 | ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-1: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT BRADYARRHYTHMIA (CARDIAC PACEMAKERS) |
DIN EN ISO 14233:2003-10 | DENTISTRY - POLYMER-BASED DIE MATERIALS |
BS EN ISO 1567:2001 | Dentistry. Denture base polymers |
ISO 14727:1998 | Dental implants Prefabricated parts connecting suprastructures to dental implants Contents of technical file |
BS EN ISO 7886-2:1997 | Sterile hypodermic syringes for single use Syringes for use with power-driven syringe pumps |
BS EN ISO 14233:2003 | Dentistry. Polymer-based die materials |
ISO 14233:2003 | Dentistry — Polymer-based die materials |
BS EN ISO 14727:1999 | Dental implants. Prefabricated parts connecting suprastructures to dental implants. Contents of technical file |
BS EN 376:2002 | Information supplied by the manufacturer with in vitro diagnostic reagents for self-testing |
BS EN 591:2001 | Instructions for use for in vitro diagnostic instruments for professional use |
EN 62298-3:2005 | Teleweb application - Part 3: Superteletext profile |
EN ISO 1567 : 2000 | DENTISTRY - DENTURE BASE POLYMERS |
ENV 1613 : 1995 | MEDICAL INFORMATICS - MESSAGES FOR EXCHANGE OF LABORATORY INFORMATION |
EN 866-1 : 1997 | BIOLOGICAL SYSTEMS FOR TESTING STERILIZERS AND STERILIZATION PROCESSES - GENERAL REQUIREMENTS |
EN ISO 14727:1998/AC:1998 | DENTAL IMPLANTS - PREFABRICATED PARTS CONNECTING SUPRASTRUCTURES TO DENTAL IMPLANTS - CONTENTS OF TECHNICAL FILE |
EN 592 : 2002 | INSTRUCTIONS FOR USE FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR SELF-TESTING |
EN ISO 14233:2003 | Dentistry - Polymer-based die materials (ISO 14233:2003) |
EN 376 : 2002 | INFORMATION SUPPLIED BY THE MANUFACTURER WITH IN VITRO DIAGNOSTIC REAGENTS FOR SELF-TESTING |
EN 867-1 : 1997 | NON-BIOLOGICAL SYSTEMS FOR USE IN STERILIZERS - GENERAL REQUIREMENTS |
04/30113078 DC : DRAFT MAY 2004 | EN 50419 - MARKING OF ELECTRICAL AND ELECTRONIC EQUIPMENT IN ACCORDANCE WITH ARTICLE 11(2) OF DIRECTIVE 2002/96/EC (WEEE) |
07/30166927 DC : DRAFT AUG 2007 | BS EN 868-3 - PACKAGING MATERIALS FOR TERMINALLY STERILIZED MEDICAL DEVICES - PART 3: PAPER FOR USE IN THE MANUFACTURE OF PAPER BAGS (SPECIFIED IN EN 868-4) AND IN THE MANUFACTURE OF POUCHES AND REELS (SPECIFIED IN EN 868-5) - REQUIREMENTS AND TEST METHODS |
CR 1750:1999 | Identification card systems - Inter-sector messages between devices and hosts - Acceptor to acquirer messages |
06/30122245 DC : 0 | EN 980 - SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
I.S. EN 61313-1:1999 | FIBRE OPTIC PASSIVE COMPONENTS AND CABLE ASSEMBLIES - PART 1: CAPABILITY APPROVAL - GENERIC SPECIFICATION |
DIN EN ISO 13897:2004-08 | DENTISTRY - AMALGAM CAPSULES |
S.R. CR 1750:1999 | IDENTIFICATION CARD SYSTEMS - INTER-SECTOR MESSAGES BETWEEN DEVICES AND HOSTS - ACCEPTOR TO ACQUIRER MESSAGES |
BS EN 592:2002 | Instructions for use for in vitro diagnostic instruments for self-testing |
EN 45502-2-2 : 2008 COR 2009 | ACTIVE IMPLANTABLE MEDICAL DEVICES - PART 2-2: PARTICULAR REQUIREMENTS FOR ACTIVE IMPLANTABLE MEDICAL DEVICES INTENDED TO TREAT TACHYARRHYTHMIA (INCLUDES IMPLANTABLE DEFIBRILLATORS) |
DIN EN 980:2003-08 | SYMBOLS FOR USE IN THE LABELLING OF MEDICAL DEVICES |
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