ARTICLE;
DEVICE SAFETY;
DEVICES;
ELECTROMAGNETIC FIELD;
EQUIPMENT;
HEALTH CARE FACILITY;
HUMAN;
INTERNET;
RADIOFREQUENCY IDENTIFICATION;
STANDARD;
WIRELESS COMMUNICATION;
ELECTROMAGNETIC FIELDS;
EQUIPMENT AND SUPPLIES;
EQUIPMENT SAFETY;
HEALTH FACILITY ENVIRONMENT;
HUMANS;
INTERNET;
RADIO FREQUENCY IDENTIFICATION DEVICE;
WIRELESS TECHNOLOGY;
ETSI EN 300 330-2 Electromagnetic Compatibility and Radio Spectrum Matters (ERM); Short Range Devices (SRD); Radio Equipment in the Frequency Range 9 kHz to 25 MHz and Inductive Loop Systems in the Frequency Range 9 kHz to 30 MHz; Part 2: Harmonized EN under Article 3.2 of the R&TTE
3
78650819107
note
ETSI EN 300220 Electromagnetic compatibility and Radio spectrum Matters (ERM); Short Range Devices (SRD); Radio equipment to be used in the 25 MHz to 1 000 MHz frequency range with power levels ranging up to 500 mW; Part 1: Technical characteristics and test methods
4
78650805279
note
ETSI EN 300 440-1 V1.5.1 (2009-03) European Standard (Telecommunications series) Electromagnetic compatibility and Radio spectrum Matters (ERM); Short range devices; Radio equipment to be used in the 1 GHz to 40 GHz frequency range; Part 1: Technical characteristics and test methods
5
78650805818
COUNCIL DIRECTIVE of 14 June 1993 concerning medical devices. Medical Device Directive MDD; 93/42/EEC; Bruxelles
COUNCIL DIRECTIVE of 14 June 1993 concerning medical devices. Medical Device Directive MDD; 93/42/EEC; Bruxelles.
6
78650830067
COUNCIL DIRECTIVE of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices. Active Implantable Medical Device Directive AIMD; 90/385/EEC; Bruxelles
COUNCIL DIRECTIVE of 20 June 1990 on the approximation of the laws of the Member States relating to active implantable medical devices. Active Implantable Medical Device Directive AIMD; 90/385/EEC; Bruxelles.
7
78650832454
COUNCIL DIRECTIVE of 27 October 1998 on in vitro diagnostic medical devices; 98/79/EC; Bruxelles
COUNCIL DIRECTIVE of 27 October 1998 on in vitro diagnostic medical devices; 98/79/EC; Bruxelles.
8
78650812054
IEC/EN 60601-1-2 Medical electrical equipment - part 1: general requirements for safety 2. collateral standard: electromagnetic compatibility - requirements and tests
IEC/EN 60601-1-2 Medical electrical equipment - part 1: general requirements for safety 2. collateral standard: electromagnetic compatibility - requirements and tests
9
67649958631
Interference with the operation of medical devices resulting from the use of radio frequency identification technology
Jun 19
Houliston B, Parry D, Webster CS, Merry AF. Interference with the operation of medical devices resulting from the use of radio frequency identification technology. N Z Med J. 2009 Jun 19;122(1297):9-16.
Testing potential interference with RFID usage in the patient care environment
Nov-Dec;
Christe B, Cooney E, Maggioli G, Doty D, Frye R, Short J. Testing potential interference with RFID usage in the patient care environment. Biomed Instrum Technol. 2008 Nov-Dec;42(6):479-84.
Electromagnetic interference from radio frequency identification inducing potentially hazardous incidents in critical care medical equipment
Jun 25
van der Togt R, van Lieshout EJ, Hensbroek R, Beinat E, Binnekade JM, Bakker PJ. Electromagnetic interference from radio frequency identification inducing potentially hazardous incidents in critical care medical equipment. JAMA. 2008 Jun 25;299(24):2884-90.
ANSI C63.18. Recommended practice for an on-site, ad hoc test method for estimating radiated electromagnetic immunity of medical devices to specific radiofrequency transmitters, IEEE 1997.