Mon, 20 Mar 2023 15:00 GMT
Europe, overview of all ETSI EN standards on approval and published from January 2023 - December 2023, not yet cited in the OJ´s.
Mon, 02 Jan 2023 08:00 GMT
Teleconformity provides FCC "Responsible Party" service for "Agent of Service for Process" under 2.911(d)7. This service is meant for foreign manufacturers (grantee's) without legal presence in the US, but requiring FCC certification for their products under one (or more) FCC ID's. It can be a long term service for one or multiple FCC ID's or an easy permanent service for just 1 FCC ID. Please contact us!
Mon, 02 Jan 2023 07:50 GMT
Teleconformity provides FCC "Responsible Party" service for part 15B sDoC "holding". This service is meant for foreign manufacturers without legal presence in the US. Instead a U.S. company is responsible for the sDoC. The 15B sDoC is for devices that contain (or not) part 15, 22/24/27 transmitters in combination with a digital portion requiring additional authorization under part 15B, in case 15B certification is not applied. We offer easy permanent services for just 1 sDoC (or more) without reoccurring payments. Please contact us!
Thu, 01 Dec 2022 14:00 GMT
Europe, overview of all ETSI EN standards on approval and published from January 2022 - December 2022, not yet cited in the OJ´s.
Fri, 01 Oct 2021 12:00 GMT
Europe, overview of all ETSI EN standards on approval and published from January 2021 - December 2021, not yet cited in the OJ´s.
Fri, 30 Jul 2021 16:00 GMT
For manufacturers located outside the European Union, Teleconformity provides legal European Authorised Entity services for Wireless and Electronic devices (RED and EMC/LVD). At present, non EU manufacturers must have a legal European Entity in place, acting as their responsive contact w.r.t. compliancy matters related to the products placed on the market, capable of liasing with frequency and market surveillance authorities throughout the European Union. Teleconformity's experience is now available to your company, handling your interests in the best possible way.
Mon, 02 Nov 2020 07:50 GMT
About adopted KDB procedures, Wireless Power Transfer Devices, Alternate measurement procedures, IECS-002 Issue 7, IECS-001 Issue 5, RSS-125 Issue 3, RSS-192 Issue 4, RSS-HAC Issue 1, TAS protocol, RSS-222 Issue 2, RSS-191 Issue 3, RSS-310 Issue 5, RSS-210 Issue 10, Applicability of IEC6209-3, January update on Electronic labelling, etc.
Mon, 05 Oct 2020 12:00 GMT
About Revision of Frequency Assignment Plan, System for the Prevertion of Radio Propagation Blockage, updated Spectrum Charts as of 1st March 2020, etc.
Thu, 01 Oct 2020 16:00 GMT
Europe, overview of all ETSI EN standards on approval and published from January 2020 - December 2020 up to today, not yet cited in the OJ´s.
Wed, 01 July 2020 14:00 GMT
Publication in accordance with Article 1(3) of Commission Decision 2000/299/EC (Version January 2020 of indicative and non-exhaustive list) In accordance with Article 1(3) of Commission Decision 2000/299/EC 1 the table below contains a list of equipment falling within the scope of ‘Class 1’.
Wed, 05 Feb 2020 12:00 GMT
Europe, implementing decision on the harmonised standards for radio equipment drafted in support of Directive 2014/53/EU.
Wed, 02 Oct 2019 08:00 GMT
Europe, overview of all ETSI EN standards on approval and published from January 2019 up to December 2019.
Wed, 18 Sep 2019 12:00 GMT
India, WPC DOT legal reference REGD.NO.D.L-33004/99 published on 2008-06-30, delicensing RFID equipment working in the 865-867 MHz band, allowing a maximum of 4 Watt erp and a 20 dB bandwidth of 200 kHz, whereas timing requirements are not specified. Spurious emission requirements are based on "not disturbing other users", thus applying international unwanted emission limits which are a direct responsibility for the manufacturer or registration holder.
Mon, 16 Sep 2019 09:00 GMT
Europe, OJ C 389 published on 17 November 2017 shows the latest harmonised Standards for the Medical Device Directive (MDD). Please note that from 25 May 2020, both the Medical Device Direcetive 93/42/EC and the directive on active implantable medical devices 90/385/EC will be fully replaced by the new Medical Device Regulation (MDR).
Fri, 14 Sep 2018 12:00 GMT
Europe, OJ C 326 published on September 14 2018 shows the latest harmonised Standards for the Radio Equipment directive (RED). The OJ is being updated frequently, so keep an eye on it in order to catch the changes timely.