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ETSI EN 302537-1-V1.1.2 20.12.2007 - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz; Part 1

Platná norma ETSI EN 302537-1-V1.1.2 Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz; Part 1: Technical characteristics and test methods

ETSI EN 302537-V2.1.1 4.10.2016 - Ultra Low Power Medical Data Service (MEDS) Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz; Harmonised Standard covering the essential requirements of article 3.2 of the Directive 2014/

Platná norma ETSI EN 302537-V2.1.1 Ultra Low Power Medical Data Service (MEDS) Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz; Harmonised Standard covering the essential requirements of article 3.2 of the Directive 2014/53/EU

DIN EN 302537 1.1.2017 - Ultra Low Power Medical Data Service (MEDS) Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz - Harmonised Standard covering the essential requirements of article 3.2 of the Directive 2014/53/EU.

Platná norma DIN EN 302537 Ultra Low Power Medical Data Service (MEDS) Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz - Harmonised Standard covering the essential requirements of article 3.2 of the Directive 2014/53/EU.

DIN EN 302537-1 1.4.2008 - Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz - Part 1: Techn

Neplatná norma DIN EN 302537-1 Electromagnetic compatibility and Radio spectrum Matters (ERM) - Short Range Devices (SRD) - Ultra Low Power Medical Data Service Systems operating in the frequency range 401 MHz to 402 MHz and 405 MHz to 406 MHz - Part 1: Technical characteristics and test methods.

Dorland's Pocket Medical Dictionary - Dorland

Since 1898, "Dorland's Pocket Medical Dictionary" has set the world standard as a handy, portable reference on medical terminology. It provides the accurate, clear, up-to-date coverage expected from Dorland's...in a highly compact, easy-to-use format. The 27th Edition features comprehensive updates that reflect all of the very latest medical terms and definitions. In addition, a new two-color page layout-with head words and guide words printed in red-makes reference even easier. What's more, th...

E DIN 13098-2 1.9.1984 - Single use syringes for medical use; syringes for power infusion apparatus.

Neplatná norma E DIN 13098-2 Single use syringes for medical use; syringes for power infusion apparatus.

DIN VDE 0558-507 1.12.2008 - VDE 0558-507. Battery based central safety power supply systems for medical electrical equipment.

Platná norma DIN VDE 0558-507 VDE 0558-507. Battery based central safety power supply systems for medical electrical equipment.

GOST 30324.31-2002 1.1.2015 - Medical electrical equipment. Part 2. Particular requirements for the safety of external cardiac pacemakers with internal power source

Platná norma GOST 30324.31-2002 Medical electrical equipment. Part 2. Particular requirements for the safety of external cardiac pacemakers with internal power source

GOST R 50267.31-99 1.1.2001 - Medical electrical equipment. Part 2. Particular requirement for the safety of external cardiac pacemakers with internal power source

Neplatná norma GOST R 50267.31-99 Medical electrical equipment. Part 2. Particular requirement for the safety of external cardiac pacemakers with internal power source

E DIN VDE 0558-507 1.10.2007 - VDE 0558-507. Battery based central safety power supply systems for medical electrical equipment.

Neplatná norma E DIN VDE 0558-507 VDE 0558-507. Battery based central safety power supply systems for medical electrical equipment.

E DIN VDE 0558-507 1.3.1996 - VDE 0558-507. Semiconductor convertors - Part 507: Battery based central safety power supply systems for medical electrical equipment.

Neplatná norma E DIN VDE 0558-507 VDE 0558-507. Semiconductor convertors - Part 507: Battery based central safety power supply systems for medical electrical equipment.

E DIN IEC 96/58/CD 1.12.1996 - VDE 0570-2-15. Safety of power transformers, power supply units and similar - Part 2-15: Particular requirements for isolating transformers for the supply of medical rooms.

Neplatná norma E DIN IEC 96/58/CD VDE 0570-2-15. Safety of power transformers, power supply units and similar - Part 2-15: Particular requirements for isolating transformers for the supply of medical rooms.

DIN EN 61558-2-15 1.11.2001 - VDE 0570-2-15. Safety of power transformers, power supply units and similar - Part 2-15: Particular requirements for isolating transformers for the supply of medical locations.(Bezpečnost výkonových transformátorů, napájecích

Neplatná norma DIN EN 61558-2-15 VDE 0570-2-15. Safety of power transformers, power supply units and similar - Part 2-15: Particular requirements for isolating transformers for the supply of medical locations.(Bezpečnost výkonových transformátorů, napájecích zdrojů a podobně - Část 2-15: Zvláštní požadavky pro oddělovací ochranné transformátory pro napájení v místnostech pro léčebné účely..)

ETSI TR 103451-V1.1.1 3.11.2016 - System Reference document (SRdoc); Short Range Devices (SRD); Technical characteristics for UHF wideband Ultra Low Power Wireless Medical Capsule Endoscopy

Platná norma ETSI TR 103451-V1.1.1 System Reference document (SRdoc); Short Range Devices (SRD); Technical characteristics for UHF wideband Ultra Low Power Wireless Medical Capsule Endoscopy

E DIN IEC 62D/206/CD-V 1.12.1996 - VDE 0750-2-31/A1. Medical electrical equipment - Part 2: Particular requirements for the safety of external cardiac pacemakers with internal power source.

Neplatná norma E DIN IEC 62D/206/CD-V VDE 0750-2-31/A1. Medical electrical equipment - Part 2: Particular requirements for the safety of external cardiac pacemakers with internal power source.

E DIN IEC 64(Sec)629 1.4.1993 - VDE 0100-710. Erections of power installations with nominal voltages up to 1000 V; electrical installations in hospitals and locations for medical use outside hospitals; identical with IEC 64(Secretariat)629.

Neplatná norma E DIN IEC 64(Sec)629 VDE 0100-710. Erections of power installations with nominal voltages up to 1000 V; electrical installations in hospitals and locations for medical use outside hospitals; identical with IEC 64(Secretariat)629.

E DIN EN 60601-2-31 1.3.2017 - VDE 0750-2-31. Medical Electrical Equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source.

Platná norma E DIN EN 60601-2-31 VDE 0750-2-31. Medical Electrical Equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source.

GOST R 52459.27-2009 1.1.2010 - Electromagnetic compatibility of technical equipment. Radio communication equipment. Part 27. Specific requirements for ultra low power active medical implants and related peripheral devices

Platná norma GOST R 52459.27-2009 Electromagnetic compatibility of technical equipment. Radio communication equipment. Part 27. Specific requirements for ultra low power active medical implants and related peripheral devices

GOST R 52459.31-2009 1.1.2010 - Electromagnetic compatibility of technical equipment. Radio communication equipment. Part 31. Specific requirements for equipment in 9 kHz to 315 kHz band for ultra low power active medical implants and related peripheral d

Platná norma GOST R 52459.31-2009 Electromagnetic compatibility of technical equipment. Radio communication equipment. Part 31. Specific requirements for equipment in 9 kHz to 315 kHz band for ultra low power active medical implants and related peripheral devices

E DIN EN 60601-2-31 1.8.1994 - VDE 0750-2-31. Medical electrical equipment - Part 2: Particular requirements for the safety of external cardiac pacemakers with internal power source.

Neplatná norma E DIN EN 60601-2-31 VDE 0750-2-31. Medical electrical equipment - Part 2: Particular requirements for the safety of external cardiac pacemakers with internal power source.

E DIN EN 60601-2-31 1.9.2007 - VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.

Neplatná norma E DIN EN 60601-2-31 VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.

DIN EN 60601-2-31/A1 1.5.1999 - VDE 0750-2-31/A1. Medical electrical equipment - Part 2-31: Particular requirements for the safety of external cardiac pacemakers with internal power source; Amendment A1.

Neplatná norma DIN EN 60601-2-31/A1 VDE 0750-2-31/A1. Medical electrical equipment - Part 2-31: Particular requirements for the safety of external cardiac pacemakers with internal power source; Amendment A1.

E DIN EN 60601-2-31/A1 1.5.2010 - VDE 0750-2-31/A1. Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source.

Neplatná norma E DIN EN 60601-2-31/A1 VDE 0750-2-31/A1. Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source.

BS EN 60601-2-31:2008+A1:2011 31.7.2009 - Medical electrical equipment. Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Zdravotnické elektrické přístroje - Část 2-31: Zvláštn

Platná norma BS EN 60601-2-31:2008+A1:2011 Medical electrical equipment. Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Zdravotnické elektrické přístroje - Část 2-31: Zvláštní požadavky na bezpečnost externích kardiostimulátorů s vnitřním zdrojem energie.)

BS EN 60601-2-31:1995 15.6.1995 - Medical electrical equipment. Particular requirements for safety. Specification for external cardiac pacemakers with internal power source(Zdravotnické elektrické přístroje - Část 2-31: Zvláštní požadavky na bezpečnost ex

Neplatná norma BS EN 60601-2-31:1995 Medical electrical equipment. Particular requirements for safety. Specification for external cardiac pacemakers with internal power source(Zdravotnické elektrické přístroje - Část 2-31: Zvláštní požadavky na bezpečnost externích kardiostimulátorů s vnitřním zdrojem energie.)

IEC 60601-2-31-ed.2.0 26.3.2008 - Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Appareils electromedicaux - Partie 2-31: Exigences

Platná norma IEC 60601-2-31-ed.2.0 Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Appareils electromedicaux - Partie 2-31: Exigences particulieres pour la securite de base et les performances essentielles des stimulateurs cardiaques externes a source d´energie interne)

IEC 60601-2-31-ed.2.1 29.9.2011 - Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Appareils electromedicaux - Partie 2-31: Exigences

Platná norma IEC 60601-2-31-ed.2.1 Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source(Appareils electromedicaux - Partie 2-31: Exigences particulieres pour la securite de base et les performances essentielles des stimulateurs cardiaques externes a source d´energie interne)

ETSI TR 102434-V1.1.1 22.6.2005 - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Alternative Interference Mitigation Technologies to Listen Before Talk (LBT) for Ultra Low Power Active Medical Implants (ULP-AMI)

Platná norma ETSI TR 102434-V1.1.1 Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Alternative Interference Mitigation Technologies to Listen Before Talk (LBT) for Ultra Low Power Active Medical Implants (ULP-AMI) operating from 403,5 MHz to 403,8 MHz with a duty cycle of less than or equal to 0,01%; System Reference Document

ETSI EN 301489-27-V1.1.1 1.6.2004 - Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 27: Specific conditions for Ultra Low Power Active Medical Implants (UL

Platná norma ETSI EN 301489-27-V1.1.1 Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 27: Specific conditions for Ultra Low Power Active Medical Implants (ULP-AMI) and related peripheral devices (ULP-AMI-P)

ETSI EN 301489-35-V1.1.2 29.10.2013 - Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 35: Specific requirements for Low Power Active Medical Implants (LP-A

Platná norma ETSI EN 301489-35-V1.1.2 Electromagnetic compatibility and Radio spectrum Matters (ERM); ElectroMagnetic Compatibility (EMC) standard for radio equipment and services; Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) operating in the 2 483,5 MHz to 2 500 MHz bands

UNE-EN 61558-2-15:2012 26.12.2012 - SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF - PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS(Bezpečnost výkonových transform

Platná norma UNE-EN 61558-2-15:2012 SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF - PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS(Bezpečnost výkonových transformátorů, napájecích zdrojů a podobně - Část 2-15: Zvláštní požadavky pro oddělovací ochranné transformátory pro napájení v místnostech pro léčebné účely.)

DIN EN 301489-27 1.7.2017 - ElectroMagnetic Compatibility (EMC) standard for radio equipment and services - Part 27: Specific conditions for Ultra Low Power Active Medical Implants (ULP-AMI) and related peripheral devices (ULP-AMI-P) - Harmonised Standard

Platná norma DIN EN 301489-27 ElectroMagnetic Compatibility (EMC) standard for radio equipment and services - Part 27: Specific conditions for Ultra Low Power Active Medical Implants (ULP-AMI) and related peripheral devices (ULP-AMI-P) - Harmonised Standard covering the essential requirements of article 3.1(b) of Directive 2014/53/EU.

DIN EN 60601-2-31 1.4.2012 - VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.(Zdravotnické elektrické přístroje - Část 2-

Platná norma DIN EN 60601-2-31 VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.(Zdravotnické elektrické přístroje - Část 2-31: Zvláštní požadavky na bezpečnost externích kardiostimulátorů s vnitřním zdrojem energie..)

DIN EN 301489-35 1.2.2014 - Electromagnetic compatibility and Radio spectrum Matters (ERM) - ElectroMagnetic Compatibility (EMC) standard for radio equipment and services - Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) oper

Neplatná norma DIN EN 301489-35 Electromagnetic compatibility and Radio spectrum Matters (ERM) - ElectroMagnetic Compatibility (EMC) standard for radio equipment and services - Part 35: Specific requirements for Low Power Active Medical Implants (LP-AMI) operating in the 2 483,5 MHz to 2 500 MHz bands.

DIN EN 301839-1 1.4.2003 - Electromagnetic compatibility and Radio spectrum Matters (ERM) - Radio equipment in the frequency range 402 MHz to 405 MHz for ultra low power active medical implants and accessories - Part 1: Technical characteristics, includin

Neplatná norma DIN EN 301839-1 Electromagnetic compatibility and Radio spectrum Matters (ERM) - Radio equipment in the frequency range 402 MHz to 405 MHz for ultra low power active medical implants and accessories - Part 1: Technical characteristics, including electromagnetic compatibility requirements, and test methods.

ETSI TR 101981-V1.1.1 20.7.2001 - ElectroMagnetic Compatibility and Radio Spectrum Matters (ERM); Short Range Devices (SRD); System Reference Document for inductive Loop - Ultra Low Power Active Medical Implants (ULP- AMI) - systems operating in the frequ

Platná norma ETSI TR 101981-V1.1.1 ElectroMagnetic Compatibility and Radio Spectrum Matters (ERM); Short Range Devices (SRD); System Reference Document for inductive Loop - Ultra Low Power Active Medical Implants (ULP- AMI) - systems operating in the frequency bands 9 kHz to 315 kHz

ETSI TR 101981-V1.2.1 19.4.2002 - Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); System Reference Document for inductive Loop - Ultra Low Power Active Medical Implants (ULP- AMI) - systems operating in the frequ

Platná norma ETSI TR 101981-V1.2.1 Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); System Reference Document for inductive Loop - Ultra Low Power Active Medical Implants (ULP- AMI) - systems operating in the frequency bands 9 kHz to 315 kHz

DIN EN 60601-2-31 1.1.2009 - VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.(Zdravotnické elektrické přístroje - Část 2-

Neplatná norma DIN EN 60601-2-31 VDE 0750-2-31. Medical electrical equipment - Part 2-31: Particular requirements for basic safety and essential performance of external cardiac pacemakers with internal power source.(Zdravotnické elektrické přístroje - Část 2-31: Zvláštní požadavky na bezpečnost externích kardiostimulátorů s vnitřním zdrojem energie..)

Survival Synephrine Fair Power 90 kapslí

Survival Synephrine Fair Power 90 kapslí Synephrine Fair Power 90 kapslíSynephrine Fair Power® je účinným pomocníkem při podpoře redukce hmotnosti a tukových zásob. Jedna drobná kapsle vám poskytne 10 mg čistého synefrinu, tj. maximální množství, které povoluje česká legislativa! Synephrine Fair Power® tak nesmí chybět v žádném suplementačním plánu všech jedinců usilujících o dokonalou postavu či maximalizaci efektu předsoutěžní diety.S oblibou používají:• rekreační sportovci• siloví sportovci...

ETSI TR 102309-V1.1.1 11.5.2004 - Electromagnetic compatibility and Radio spectrum Matters (ERM); Ultra Low Power Active Medical Implants (ULP-AMI); Membrane Implant devices operating in the 30 MHz to 37,5 MHz band; System Reference Document

Platná norma ETSI TR 102309-V1.1.1 Electromagnetic compatibility and Radio spectrum Matters (ERM); Ultra Low Power Active Medical Implants (ULP-AMI); Membrane Implant devices operating in the 30 MHz to 37,5 MHz band; System Reference Document