MEDICAL DEVICES SERVICES FOR CE MARKING WITH ITS PARTNER EUROPEAN NOTIFIED BODY
The icon displayed at the top of this page is the CE mark. The word "Conformité Européene," which translates to "European Conformity" in French, is abbreviated as "CE." First used in Directive 93/68/EEC, the term "EC mark" was formally replaced by "CE mark" in 1993. In all official EU papers, the "CE Mark" is now utilized.
The maker certifies that a product carries the CE mark by stating that it complies with all pertinent European health, safety, and environmental regulations. However, there are actually a lot of so-called products out there. in accordance with product instructions. The "essential requirements" and/or "performance levels" and "harmonized standards" that products must adhere to are specified in product directives.
We are glad to share with you the details of our partnership/cooperation with the European Notified Body through BSCIC Certifications Pvt. Ltd. Medical device certification according to the MDR. Currently, the new Medical Device Regulation (MDR) (EU) is being implemented. We would provide CE Mark certification services for medical products through this agreement to the Indian and UAE markets.