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Network
- inetnum : 199.59.243.0 - 199.59.243.255
- name : BODIS-A
- handle : NET-199-59-243-0-1
- status : Reassigned
- created : 2010-09-27
- changed : 2021-10-16
Owner
- organization : Bodis, LLC
- handle : BODIS-1
- address : Array,Tampa,FL,33609,US
Technical support
- handle : BODIS1-ARIN
- name : Bodis Administrator
- phone : +1-877-263-4744
- email : [email protected]
Abuse
- handle : BODIS2-ARIN
- name : Bodis Abuse
- phone : +1-877-263-4744
- email : [email protected]
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Host Informations
- IP address: 199.59.243.225
- Location: United States
- Latitude: 37.751
- Longitude: -97.822
- Timezone: America/Chicago
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Websites Listing
We found Websites Listing below when search with devises.eu on Search Engine
ZTE - Official Website | Axon 40 Ultra ( Europe ) – ZTE EU
ZTE is the global leader in telecommunications with a vision towards tommorow and is committed to creating tommorows technology, today. ZTE are accelerating it's global …
Eu.ztedevices.comEU devises new measures against 'economic coercion'
2021-12-10 · Europe EU devises new measures against 'economic coercion' The carrot, or the stick? The European Commission no longer wants to put up with economic blackmail such as …
Dw.comMedical Devices - EUDAMED
EUDAMED is the IT system developed by the European Commission to implement Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746….
Health.ec.europa.euUDI/Devices registration - Public Health
Regulation (EU) 2017/745 on medical devices and Regulation (EU) 2017/746 on in vitro diagnostic medical devices introduce an EU device identification system based on a unique …
Health.ec.europa.euGerman national requirements for medical devices - MDlaw
2021-09-28 · The Medical Devices EU Adaptation Act (MPEUAnpG) and the Medical Devices Implementation Act (MPDG) The new Regulation (EU) 2017/745 (MDR) entails adaptation …
Mdlaw.euDistributors – The European Union Medical Device Regulation
If your company is established in a country outside the EU it is not considered by the EU MDR. The distributors referred to in Article 14 and elsewhere in the EU MDR, are distributors who …
Eumdr.comHarmonised standards - Public Health
2022-05-17 · Harmonised standards under the medical devices Regulations are developed by CEN and CENELEC as European standardisation organisations, on the basis of a …
Health.ec.europa.euTest results - European Central Bank
2022-07-01 · Introduction. This page provides a regularly updated list of tested banknote authentication devices to help you choose the counterfeit detection equipment most suitable …
Ecb.europa.euEU IVDR – Regulation (EU) 2017/746 - The European Union In Vitro ...
Publication of COM (2021)627 Regulation of the European Parliament and of the Council amending Regulation (EU) 2017/746 as regards transitional provisions for certain in vitro …
Euivdr.comEUDAMED - European Commission
The creation of a European database on medical devices (EUDAMED) is one of the key aspects of the new rules on medical devices ( Regulation (EU) 2017/745) and in vitro diagnostic …
Ec.europa.euVolkswagen defeat devices were illegal in certain driving …
2022-07-14 · Volkswagen AG software that altered car emissions constituted an illegal defeat device in certain driving conditions, the EU’s top court ruled on Thursday, while the automaker …
Theglobeandmail.comEU Medical Devices Regulations Information Center | SGS
Here you will find some important documents to guide you in an application for certification against the new Medical Devices Regulation and In Vitro Diagnostic Medical Device Regulation.
Sgs.comRisk Management for Medical Devices under EU MDR and ISO 14971
2022-05-19 · Risk management is required by law through the European Regulation (EU) 2017/745 on medical devices (MDR), to ensure that medical products are safe for patients, …
Decomplix.comEU Importer of Medical Devices - MDR / IVDR - Kinesis Medical
EU importer of medical devices. If you are looking to expand your business by exporting your medical device to Europe, you have to comply with the new Medical Device Regulation (EU) …
Kinesismedical.comAll Products – ZTE EU
ZTE is the global leader in telecommunications with a vision towards tommorow and is committed to creating tommorows technology, today. ZTE are accelerating it's global commercial …
Eu.ztedevices.comMedical Devices and GDPR (the EU General Data ... - StarFish Medical
2018-02-01 · With an enforcement date of May 25, 2018, the European Union (EU) General Data Protection Regulation (GDPR) is about to impact medical device manufacturers. Though …
Starfishmedical.comMobile devices | European Data Protection Supervisor
2022-06-16 · This is one element of an acceptable-use policy on mobile devices which lays down the rules for their professional use. Where Bring-Your-Own-Devices (when private devices are …
Edps.europa.euMDR Labelling Requirements - Medical Device Regulation
8 Information for Users (Labeling/IFU) •IFU Requirements (23.4) •New requirement for implantables –include qualitative & quantitative information on materials and substances …
Medical-device-regulation.euANNEX XVI - Medical Device Regulation
2019-08-14 · High intensity electromagnetic radiation (e.g. infra-red, visible light and ultra-violet) emitting equipment intended for use on the human body, including coherent and non-coherent …
Medical-device-regulation.euIv diagnostic medical devices old - European Commission
Short name: In vitro diagnostic medical devices. Base: Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices OJ L …
Ec.europa.eu
Domains Expiration Date Updated
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|---|---|---|
| isbndb.com | godaddy.com | -1 Years, -234 Days |
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