CE Marking Service for Medical Devices in Punjab, Ludhiana, Amritsar, Barnala, Bathinda, Fazilka, Faridkot, Fatehgarh Sahib, Firozpur, Gurdaspur, Hoshiarpur, Jalandhar, Kapurthala, Mansa, Moga, Mohali, Muktsar, Pathankot, Patiala, Rupnagar, Sangrur, Shahid Bhagat Singh Nagar, Tarn Taran
Eurotech Certification Body Providing Guidelines for Classification of Medical Devices – CE Marking (CE Mark) for Medical Devices – EU Council Directive 93/42/EEC, Gain market access in Europe with a CE mark: Sell your medical devices in Europe with advice and a free e-update service, Eurotech offers services required under the European Union Medical Device Directive, 93/42/EEC, including the auditing of a manufacturer’s quality system.
Eurotech is a leading notified body for the Medical Devices Directive and the In-Vitro Diagnostic (IVD) Devices Directive. We provide conformity assessment services and CE Certification under all device classifications.
CE Marking for Medical Devices. Eurotech provides comprehensive testing and certification services, guiding you through every step of the CE Marking process Medical device manufacturers to understand and comply with the MDD and CE-marking requirements. Numerous discussions with clients, auditors and experts
People also ask:
Q:- What is the benefit to the user of the CE symbol?
Q:- What is the CE Marking on medical devices?
Q:- What is the CE mark?
Q:- Is my product a Medical Device (MD) or In Vitro Diagnostic Medical Device (IVD)?
Q:- Which category does an In Vitro Diagnostic Medical Device (IVD) fall into?
Q:- Why must a medical device manufacture appoint a European Authorized Representative?
Q:- In order to commercialize medical and in vitro diagnostic devices in the European Union, Q:- manufacturers must obtain CE Mark certification as part of their device
Q:- In order to commercialize medical and IVD devices in the European Union, a CE Mark certificate is needed. This certification verifies that a device meets all
Q:- How to conform with the legal requirements for placing medical devices on the market.
Q:- Do you have a question about medical devices, or about CE marking for a medical device? Find the answer on the website of notified certification body
Getting CE Marking for Medical Devices in Europe
Interested Manufacturers , Suppliers, Traders, Exporters can drop their requirements with product technical details at (CE.Marking.Certification@Gmail.Com)
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CE Marking India, CE requirements, CE certification, CE approval, Testing, EU Directives and Standards 