CE marking

CE marking is a mandatory conformity marking for certain products sold within the European Economic Area (EEA) since 1985. The CE marking is also found on products sold outside the EEA that are manufactured in, or designed to be sold in, the EEA. This makes the CE marking recognizable worldwide even to people who are not familiar with the European Economic Area. It is in that sense similar to the FCC Declaration of Conformity used on certain electronic devices sold in the United States.

The CE marking is the manufacturer's declaration that the product meets the requirements of the applicable EC directives.

The mark consists of the CE logo and, if applicable, the four digit identification number of the Notified Body involved in the conformity assessment procedure.

"CE" originated as an abbreviation of Conformité Européenne, meaning European Conformity, but is not defined as such in the relevant legislation. The CE marking is a symbol of free marketability in the European Economic Area (Internal Market).

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Latest News for: ce marking

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MultiSensor AI Announces Strategic Collaboration with FOTRIC to Drive Rapid Growth in Sensors and Solutions Businesses

ACCESSWIRE 02 Apr 2025
Inc. ("FOTRIC") ... About FOTRIC Inc ... 9001, FCC, CE, and KC certifications. Our leadership in the industrial sensing equipment sector is marked by a commitment to continuous innovation, integrating advanced technologies for comprehensive safety solutions.
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J&J MedTech Unveils Promising 12-Month Data on Dual Energy Ablation Technology at EHRA 2025

Pharmiweb 01 Apr 2025
Author Company. J&J MedTech Author Name ... The device received CE mark approval earlier this year, and while it is not yet available in the United States, the results position it as a notable development in electrophysiology innovation. Source ... .
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Johnson & Johnson MedTech Presents Pivotal 12-Month Effectiveness and Safety Data from SmartfIRE Study at 2025 EHRA Congress

Pharmiweb 01 Apr 2025
It received the European CE Mark approval in December 2024; it is currently investigational in the United States ... Primary endpoints were met at the 3-month follow up[2] ... · 40.8% relative reduction in CV-related hospitalizations compared to baseline ... Dr.
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Abbott Receives CE Mark for its Volt™ Pulsed Field Ablation System to Treat Patients with Abnormal Heart Rhythms

Pharmiweb 31 Mar 2025
CE Mark approval for the Volt PFA System was granted based on strong results from Abbott's Volt CE Mark study, a global clinical trial conducted at centers in Europe and Australia.
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Nanox Announces Fourth Quarter Of 2024 Financial Results And Provides Business Updates

MENA FN 31 Mar 2025
(MENAFN - GlobeNewsWire - Nasdaq) Recorded noted regulatory successes with FDA general use clearance and granting of CE Mark in the EU Advanced commercialization globally, signing new customer and ... .
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MAJOR BREAKTHROUGH IN RESPIRATORY DIAGNOSTICS SET TO TRANSFORM NHS LUNG CARE

Pharmiweb 31 Mar 2025
N-Tidal™ Diagnose has been granted regulatory clearance and is CE-marked under EU Medical Device Regulations for the diagnosis of COPD and is now being rolled out across GP practices across the country.
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Impulse Dynamics Receives European CE Mark For Expanded Indication For Diastolic Heart Failure

Enid News & Eagle 28 Mar 2025
Marlton, NJ, March 28, 2025 (GLOBE NEWSWIRE) -- Impulse Dynamics plc, a global medical device company dedicated to improving the lives of people with heart failure (HF), is proud to announce that it received European CE Mark approval for an ... .
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CE Europa, bringing identity, passion, and pride back to Gràcia

Catalan News 27 Mar 2025
CE Europa was founded in 1907, and became a founding member of the professional Spanish football league, La Liga, in 1929, alongside the likes of Barça, Real Madrid, and Espanyol.  ... CE Europa, ...
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Rare Buddhist seal discovered at Ratnagiri

The Times of India 27 Mar 2025
... in Jajpur district, marking a significant discovery in Buddhist archaeology.The seal, dating back to the 5th century CE, contains a Dharani Mantra written in Sanskrit using late Brahmi characters.
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FDA Issues Nyxoah an Approvable Letter for its Genio® System

Pharmiweb 26 Mar 2025
This decision does not impact Genio's CE Mark or ongoing commercial activities in Europe, where the device is approved for both Complete Concentric Collapse (CCC) and non-CCC patients ... Caution – CE marked since 2019.
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E-bikes are banned from London Tube and rail services because they keep catching fire | ...

The Daily Mail 26 Mar 2025
The fire was put out by crews from London Fire Brigade ... Mr Khan said ... Pictured ... Consumers buying any product can check that the item displays a UKCA or CE mark that ensures that the products meet UK and EU safety, health or environmental requirements ... .
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Latent TB Testing Market to Reach USD 773.4 Million by 2029, Driven by Advancements in ...

GetNews 26 Mar 2025
(China), Sanofi (France), Endo, Inc. (US), bioMérieux (France), SD Biosensor, INC ... In February 2023, its QuantiFERON-TB Gold Plus test received CE marking under the European Union's IVDR regulation, reinforcing its leadership in the market ... (China) ... Ltd.
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