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CE Certificate

Time: 2024-01-09 Source: Certificate Author: Cassie
Characteristics, Specific Meanings, and Clarifications
  • Legal Attributes: Mandatory regulatory access. Products without the CE mark or that do not meet the requirements may not be sold or used in the EU market, otherwise they will face legal sanctions.
  • Issuing Body: Not issued by a specific "CE body." The manufacturer is the declarant. For high-risk products (such as medical devices and machinery), a conformity assessment and certificate must be issued by an EU notified body before the manufacturer can affix the CE mark.
  • Certificate Target: Specific product model or series. Proof that the product model has passed the corresponding conformity assessment procedure.
  • Focus: Basic safety requirements, not quality or performance. It represents that the product, under normal use, will not pose an unacceptable danger to users, pets, property, and the environment. It is the minimum legal threshold, not a mark of excellent quality.
  • Comparison with Previous Certificates: Unlike GMP: GMP is a production qualification; CE is product market access.
  • Unlike ISO: ISO is a voluntary management system; CE is a mandatory product regulation.
  • Similar to NSF: Both are marks indicating that a product meets specific requirements, but CE is legally mandatory (EU), while NSF is authoritative and voluntary (global market).
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