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COFEPRIS Mexico Medical Device Labeling

COFEPRIS Mexico Medical Device Labeling

Medical devices sold in Mexico must have a label that communicates the information necessary to safely use the device.

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CANADian Market information

Medical device labeling in Mexico

Medical device labeling requirements in Mexico are defined by COFEPRIS, Mexico’s medical device regulator. NOM-137-SSA1-2008 is the Mexican standard that outlines the minimum requirements for medical device labeling. In 2024, COFEPRIS released a draft revision of the labeling standard, NOM-137-SSA1-2024. The revision aligns with international labeling requirements under FDA, EU MDR, IVDR, and the International Medical Device Regulators Forum (IMDRF).

Medical devices sold in Mexico must have a label that communicates the information necessary to safely use the device. Labels must be in Spanish, with the exception of the device trade name. The label should be affixed to the device itself or its packaging. The label design should be included with your registration submission to COFEPRIS; and printed labels must align with your approved label design.

Information to include in your medical device label in Mexico

Medical device labels should include the following information:

  • Generic name of the product
  • Distinctive name of the product
  • Manufacturer's data
  • Country of origin
  • Sanitary Registration number
  • The expiry date of the product, when applicable
  • Batch number or serial number
  • Quantity
  • Any adverse incident that may occur from use of the product, when applicable
  • Warning or caution legends
  • Legends of sterility
  • "Non-toxic," "pyrogen-free," or allusive legends, where applicable
  • Single use, reusable, etc. using allusive legends or corresponding symbol
  • Symbols for units of measurement
  • Declaration of their active ingredients or drugs contained, when applicable

Instructions for Use (IFU) requirements for medical devices in Mexico

Instructions for Use contain essential information about how to properly and safely use the device. You must include a printed copy of your IFU. However, the new draft NOM for labeling will allow electronic IFU in acceptable formats, as long as electronic IFU is suitable to the target population and clinical setting for the intended use of the device.

How We Can Help

Sell your medical device in Mexico

Pure Global provides medical device regulatory consulting for all aspects of COFEPRIS registration in Mexico, including medical device labeling compliance. We can ensure your medical device labeling meets COFEPRIS requirements, and help you secure market authorization in Mexico. Contact us to get started.

Frequently
Asked Questions

How are IVDs classified in Mexico?

The back label or secondary label is a supplemental label that can be added to your device to comply with labeling requirements in Mexico. NOM-137 allows for medical devices to be imported with their original label that may not be to Mexican labeling standards as long as there is a compliant secondary label.

Do low-risk medical devices still require COFEPRIS registration?

Your MRH may need to submit a modification to your application with the updated label design. Modifications can take several months to review and approve.

Single Process,
Multiple Markets

When you partner with Pure Global, a single registration process opens doors to multiple countries. Our global subsidiaries make this streamlined path possible.

Let's Talk,
Anywhere You Are.

Whether looking for more information or ready to partner with us, we're here to guide you through every step of the regulatory process.

Contact us