CE Mark definition

CE Mark means a certification mark that indicates conformity with health, safety, and environmental protection standards;

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CE Mark means Conformité Européene Mark.

CE Mark means that the boat complies with all applicable European

Examples of CE Mark in a sentence

• The Subscriber shall use the terminal device in compliance with the technical standards established by the applicable laws and regulations equivalent to the Federal Communications Commission (FCC) rules or the CE Marking (CE Mark) for Radio Telecommunications Equipment, and supported by SORACOM Air Global Service.

• The Subscriber shall use the terminal device in compliance with the technical standards established by the applicable laws and regulations equivalent to the Federal Communications Commission (FCC) rules or the CE Marking (CE Mark) for Radio Telecommunications Equipment, and supported by SORACOM Arc Service.

• Orchestra will be responsible for obtaining Regulatory Approvals required for the Clinical Trial and Medtronic will be responsible for seeking FDA, CE Mark, and PDMA Regulatory Approvals for the Commercial Device as per the Regulatory Plan.

• Exogen shall use its diligent efforts to obtain and maintain ISO 9000 certification and the CE Mark of Approval for the SAFHS 3000 device at Exogen's expense.

• Exogen warrants and represents to S&N that t▇▇ SAFHS 2000 device complies with International Standards Organization ("ISO") Certification 9003 and the Medical Device Directive and received the CE Mark of Approval on March 24, 1998, and that such certification an▇ ▇pproval will be maintained in full force and effect at Exogen's expense.

More Definitions of CE Mark

CE Mark means a marking by which a manufacturer indicates that a medical device is in conformity with the applicable requirements set out in all applicable Requirements of Law providing for its affixing.

CE Mark means the mark of conformity with one or more applicab▇▇ ▇irectives of the ▇▇▇▇pean Union.

CE Mark means Conformite Europeenne Mark or any other designation indicating that all pertinent European Community legal requirements for a medical device have been met enabling the manufacture and sale of the device in any member country.

CE Mark means, with respect to any Product, the “CE” mark issued upon approval of such Product by the European Union Regulatory Authority.

CE Mark means verification that the relevant product or process complies with all applicable European Commission requirements and, if stipulated in any directive, has had such product or process examined by a notified conformity assessment body.

CE Mark means ▇▇▇ "CE Mark" referen▇▇▇ in the Medical Device Directive and required to be placed on medical devices (including, without limitation, the Products) to be sold in the European Union after June 14, 1998.

CE Mark means a quality registration to sell certain products in the European Union.