NexorTest Technologies

NexorTest Technologies Pvt Ltd provides ISO/IEC 17025 accredited EMC/EMI Testing, Environmental Testing, Regulatory Consultation and Product Design Services to industries across North America and the Asia Pacific. Our state-of-the-art facilities and expert team ensure your products meet regulatory compliance, enhancing safety, and reliability. We cater to industries such as aerospace, defense, automotive, medical devices, wireless, and many more. With quick turnarounds time, experienced team members, competitive pricing, and customized solutions, we help you achieve global certification with confidence.

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India Medical Device Labelling Update 2026

If you sell medical devices in India, your labelling rulebook has changed twice in less than a year. The Legal Metrology (Packaged Commodities) Amendment Rules, 2025 came into force in October 2025 and ended the old dual-labelling problem. The Legal Metrology (Packaged Commodities) Amendment Rules, 2026 follow next, with two more changes lined up for 01 July 2026 and 01 July 2027. 

Now that we are in mid-2026, the real question is whether your labels, your e-commerce listings and your SOPs are aligned with the new framework. Here is a 2026 status check. 

Where the rules stand today, June 2026?

As of today, the labelling of any medical device sold in India is governed by the Medical Devices Rules, 2017. The October 2025 amendment, notified under section 52(2)(j) and (q) of the Legal Metrology Act, 2009, inserted three provisos into the Legal Metrology (Packaged Commodities) Rules, 2011. 

Rule 2(h): Declarations on medical device packages are made under MDR 2017, not the LMPC list. 

Rule 7(2): The height and width of letters and numerals on medical device labels follow MDR 2017, not the LMPC millimeter table. 

Rule 33: The general LMPC relaxations do not apply where MDR 2017 applies. No shortcuts. 

In practice, MDR 2017 Rule 46 and Schedule IV are now the single source of truth for declarations such as unique device identification, sterility, manufacturer details, batch number, expiry and use instructions. 

What is coming on 01 July 2026?

The Legal Metrology (Packaged Commodities) Amendment Rules, 2026 were notified under G.S.R. 128(E) in February 2026. They take effect on 01 July 2026. The headline change is e-commerce focused. Every e-commerce entity listing imported products must display the country of origin and make it searchable and sortable on the product listing page. 

For medical device companies selling imported devices through Indian e-commerce platforms, this is now a labelling and listing obligation that sits on top of MDR 2017. Your physical label stays under MDR. Your digital listing needs the country of origin tag and filter. 

And what is coming on 01 July 2027?

The Legal Metrology (Packaged Commodities) Second Amendment Rules, 2026 were notified in April 2026 and take effect on 01 July 2027. They substitute sub-rule 10A of Rule 6 and tighten the e-commerce country of origin disclosure further. Medical device importers using marketplaces should plan their listing template once and be ready for both 2026 and 2027 dates. 

There is also a 2026 update to the Legal Metrology (General) Rules that brings Clinical Electrical Thermometers for continuous measurement into formal verification scope, which is worth flagging if you sell continuous-temperature monitoring devices. 

Your 5-point action checklist for June and July 2026 

Audit every SKU label against MDR 2017 Rule 46 and Schedule IV. Drop LMPC-only typography rules from your label artwork brief. 

Refresh your Device Master File and SUGAM portal entries to reflect the new label artwork. 

If you sell imported devices on Indian e-commerce platforms, add a clear country of origin tag and ensure the platform listing supports a searchable filter before 01 July 2026. 

Train customs, warehouse and customer service teams on the one-rulebook position. Field inspectors are still catching up. 

Plan a second pass for 01 July 2027 so the e-commerce listing template, not just the label, is ready. 

Why this matters in the broader India picture? 

Read alongside the draft Medical Devices (Amendment) Rules, 2026 under G.S.R. 270(E) and the CDSCO Draft Guidance on Medical Device Software, the direction is clear. India is consolidating medical device compliance under MDR 2017 across labelling, testing, software and e-commerce. Companies that update once, properly, will avoid two more rounds of rework. 

Need a 2026 label and listing review under MDR 2017? 

NexorTest helps manufacturers and importers with medical device label artwork review, MDR 2017 compliance assessment, e-commerce listing alignment for the 01 July 2026 and 01 July 2027 dates, CDSCO inspection preparedness and full regulatory documentation. Visit www.nexortest.com or our India CDSCO Medical Device Registration page to start a structured review.

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EU MDR: Comprehensive Breakdown of Its Rules & How It Effects The Manufacturers

The European Union Medical Device Regulation (EU MDR) (2017/745) sets out an extensive framework that regulates the manufacture and sale of medical devices in the EU. Enacted in 2017, the EU MDR superseded the erstwhile Medical Devices Directive (MDD) (93/42/EEC) and the Active Implantable Medical Devices Directive (AIMDD) (90/385/EEC). The main goal of the EU MDR is to increase patient safety by enforcing rigorous standards upon the manufacturers of medical devices.

Key Changes Introduced by EU MDR

The MDR came into force on 26th May 2017 and became applicable on 26th May 2021 in all EU member states. The EU MDR brought some major changes to the regulatory framework:

Increased Scope: The regulation now covers a wider scope of products, including those that do not have a medical intent but share similar features with medical devices, like cosmetic implants and contact lenses.

Redesignation of Devices:A large number of devices have been redesignated into higher-risk classes, which require more stringent assessment processes.

Unique Device Identification (UDI): Each device is to be assigned a UDI by manufacturers, which facilitates better traceability in the supply chain.

Clinical Evaluation: Greater emphasis on clinical data, under which manufacturers have to supply solid clinical evidence for the safety and performance of the devices.

Post-Market Surveillance: Manufacturers need to establish good post-market surveillance systems to keep track of the performance of devices and report any adverse events.

CE Marking Under MDR

Acquiring the CE marking is a matter of law for placing medical devices on the EU market. The process of obtaining CE marking has become more rigorous under the EU MDR. Manufacturers are required to verify that their products conform to the General Safety and Performance Requirements (GSPR) of the regulation.

This entails a careful conformity assessment, possibly involving the services of a Notified Body, particularly for higher-risk devices. CE marking shall be attached visibly, legibly, and permanently to the device or on its packaging before it is made available for sale on the market.

Effects on Manufacturers

The adoption of the EU MDR has fundamental effects on the manufacturers of medical devices: Added Compliance Costs: Compliance with the new legislation entails heavy investment in quality management systems, clinical trials, and personnel training. Additional requirements translate to higher operating expenses.

Regulatory Uncertainty: The switch from the MDD to the EU MDR has created uncertainties, mainly related to how to interpret some of the provisions and the availability of Notified Bodies. Such uncertainty may lead to increased time to introduce products onto the market.

Market Entry Barriers: Small and medium-sized companies, and also manufacturers, will find it hard to comply with the strict standards, and they might be restrained from competing within the EU market.

Supply Chain Changes: UDIs and enhanced traceability compel manufacturers to shift their supply chain activities in such a way that all economic players are compliant with the regulation.

Compliance Measures

Manufacturers can navigate the challenges of the EU MDR by following the below steps:

Device Classification: Categorize the medical device based on its intended use and inherent hazards.

Quality Management System (QMS): Develop a QMS based on ISO 13485 guidelines to control processes efficiently.

Clinical Evaluation: Perform rigorous clinical evaluations to collect evidence of safety and performance of the device.

Technical Documentation: Prepare technical documentation with details of design, manufacturing procedures, and compliance with GSPR.

Work with Notified Bodies: Engage with notified Notified Bodies for conformity assessments, particularly for high-risk devices.

Post-Market Surveillance: Establish systems to follow up on the performance of devices after market placement and create reporting procedures for adverse events.

Role of Nexortest Technologies

Nexortest Technologies is one of the biggest solution partners to companies involved in maintaining compliance with the EU MDR. Possessing extensive experience in the field of regulatory consulting and compliance services Nexortest Technologies provides a list of services specialized in addressing the specific needs of the EU MDR.

Regulatory Consulting: EU MDR offers professional consultancy for the interpretation and enforcement of the requirements and facilitates better understanding and enablement of the manufacturers to meet them.

Quality Management Systems: Installing and implementing strong QMS according to ISO 13485 standards and maintaining consistent quality and compliance.

Clinical Evaluation Support: Providing consultancy services in the establishment and administration of clinical evaluation, helping in the procurement of required clinical evidence.

Technical Documentation Preparation: Facilitating preparation of in-depth technical documentation, a primary requirement for CE marking under MDR.

Training and Education: To train manufacturers through the use of workshops and training modules so that they are well aware of the new regulatory developments and best practices.

Factory Inspection (Where Necessary)

BIS officers, in the case of specific groups, carry out an inspection at the production premises to check against necessary standards.

Review and Issue of Certificate

BIS evaluates the application form, test reports, and findings of inspection.

If the terms are satisfactory, the BIS certificate is given.

Through the use of services offered by Nexortest Technologies, companies will better be able to handle the intricacy of the EU MDR so that their medical devices will be optimally suited to pass the rigorous CE marking in compliance with MDR.

Conclusion

EU MDR is a paradigm shift in the regulatory regime of medical devices in the European Union. Even though its central purpose is patient safety and performance improvement of the device, it also presents great challenges to industry manufacturers.

Compliance is achieved through a thorough knowledge of the regulations, a lot of resources, and, in most instances, partnerships with experienced companies such as Nexortest Technologies. Foreseeing and careful preparation are the key to manufacturers surviving this complicated regulation environment and sustaining access to the EU market.

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NexorTest Technologies | Expert EMI Testing Services in Bengaluru

NexorTest Technologies is a leading provider of EMI Testing Services in Bengaluru, offering ISO/IEC 17025 accredited testing and expert regulatory consultation. We cater to industries such as aerospace, defense, automotive, and more, ensuring your products meet global compliance standards, including CE, BIS, FCC, and USFDA-MDR certifications. To learn more about our EMI testing services, visit

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NexorTest Technologies | Global Testing Company

NexorTest Technologies Bengaluru offers comprehensive testing services, specializing in EMI/EMC testing, environmental testing, product design and regulatory consultation. With ISO/IEC 17025 accreditation, our expert team provides top-tier solutions to industries such as aerospace, defense, automotive, and medical devices. Based in Bengaluru, we ensure compliance with global standards, including CE, BIS, FCC, and USFDA-MDR certifications, delivering reliable results and quick turnarounds. For more information visit us

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NexorTest Technologies | Environment Testing Services in Bengaluru

NexorTest Technologies, a top Environmental Testing Certification company in Bengaluru. We offer ISO/IEC 17025 accredited testing services to industries like aerospace, defense, automotive, and medical devices. With certifications including CE, BIS, FCC, and USFDA-MDR, we ensure your products meet global compliance standards. Contact us today!

Get EMC/EMI testing services by NexorTest. Certified solutions for industrial testing, including electronics, medical, aerospace, defence,

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CE Marking: Guide for Manufacturers Seeking EU Market Access

CE marking, short for "Conformité Européenne" (French for "European Conformity"), is a mandatory symbol that indicates a product complies with the European Union's health, safety, and environmental protection standards. This marking is essential for products sold within the European Economic Area (EEA). By affixing the CE mark, manufacturers declare that their products meet all applicable EU directives and regulations, allowing for the free movement of goods across EEA countries. It's important to note that the CE mark is not a quality indicator or certification mark; rather, it signifies legal compliance with EU legislation.

The CE marking process involves several key steps to ensure that a product complies with European Union (EU) regulations and can be legally sold within the European Economic Area (EEA). Here's a step-by-step breakdown:

1. Identify Applicable Directives and Regulations:

Determine which EU directives or regulations apply to your product. Each directive outlines specific requirements related to safety, health, and environmental protection. For example, medical devices are governed by the Medical Devices Directive (MDR 2017/745).

2. Assess Specific Requirements:

Understand the essential requirements stated in the applicable directives. This may involve conducting a risk analysis and ensuring your product meets performance and safety standards.

3. Determine the Conformity Assessment Procedure:

Decide whether your product requires assessment by a Notified Body—a third-party organization authorized by the EU to evaluate product conformity. Not all products need this; some can be self-assessed by the manufacturer.

4. Conduct Product Testing:

Perform necessary tests to verify that your product meets EU requirements. Depending on the product and applicable standards, this testing can be done by an ISO 17025 accredited laboratory.

5. Compile Technical Documentation:

Gather comprehensive documentation detailing your product's design, manufacturing process, and compliance with relevant standards. This technical file should include:

Product description

Design and manufacturing drawings

Risk assessments

Test reports

User manuals

Declarations of conformity

6. Draft and Sign the EU Declaration of Conformity:

Prepare a document in which you, as the manufacturer or authorized representative, declare that the product complies with all relevant EU directives. This declaration must include:

Manufacturer's name and address

Product details (e.g., model, type)

List of applicable EU directives

Standards used to verify compliance

Date and place of issuance

Name and signature of the responsible person

7. Affix the CE Marking:

Once all the above steps are satisfactorily completed, affix the CE marking to your product. Ensure the marking is:

Visible, legible, and indelible

At least 5 mm in height (unless specified otherwise)

Proportional if resized If a Notified Body was involved, include their identification number alongside the CE mark.

By following these steps diligently, manufacturers can ensure their products meet EU standards and are eligible for sale within the EEA.

Why Choose NexorTest Technologies for CE Marking Certification?

We simplify the CE marking process with step-by-step guidance.

Our experts identify the right EU directives and standards for your product.

Save costs with our in-house accredited testing lab.

Tailored solutions ensure your product meets all CE requirements.

From compliance checks to affixing the CE mark, we manage it all.

Our streamlined process saves time and eliminates complexity.

Ensure EU regulatory compliance with precision and confidence.

Seamless market access and enhanced product credibility guaranteed.

Gain a competitive edge with our reliable support.

Contact NexorTest Technologies today to achieve hassle-free CE certification!