The New EU ESPR Regulation Is Here




The New EU ESPR Regulation Is Here: Fully Replacing Ecodesign – Will Every Product Be Affected?

For more than a decade, when companies thought of EU product energy-efficiency and environmental rules, the first thing that came to mind was the Ecodesign Directive 2009/125/EC.

But from 2024 the EU officially launched a new, more ambitious regulation with far deeper impact:

ESPR (Ecodesign for Sustainable Products Regulation). This regulation will gradually replace the old Ecodesign framework and become one of the core gateway regulations for entering the EU market in future.

For manufacturers exporting to the EU, this is not just a regulatory update but a complete restructuring of product design logic. This article systematically explains:

  • The key differences between ESPR and the old Ecodesign Directive

  • Implementation milestones

  • The impact on companies in different industries

  • What companies need to prepare in advance

1. What is ESPR, and why is the EU introducing it?

ESPR is one of the core regulations of the EU Green Deal and the Circular Economy Action Plan. The EU’s goal is very clear: climate neutrality by 2050, which means products must meet sustainability requirements from the design stage onwards.

The old Ecodesign Directive mainly addressed:

Whether a product saves energy

ESPR, by contrast, addresses:

Whether a product is sustainable throughout its entire life cycle, from raw materials → production → use → end of life

Therefore:

ESPR ≠ an upgraded energy-efficiency regulation; it is a fundamental change in the logic of EU product regulation.

2. Key differences between ESPR and Ecodesign (the old directive)

1) Different legal nature

As a Regulation, ESPR must be applied simultaneously in all Member States once in force, leaving companies no room for national transition.

2) Different product scope (the biggest change)

The Ecodesign era (old)

Applied only to energy-related products (ErP)

For example:

  • Household appliances

  • Electric motors

  • Air conditioners

  • Displays

  • Power supplies

  • Lighting

Medical and laboratory equipment were largely out of scope.

The ESPR era (new)

ESPR covers:

Almost all physical products

Including:

  • Electronics

  • Medical devices

  • IVD equipment

  • Laboratory equipment

  • Furniture

  • Textiles

  • Construction materials

  • Industrial equipment

  • Consumer goods

In other words:

Any product exported to the EU in future may be brought within the scope of ESPR

This is a fundamental change.

3. New core regulatory requirements under ESPR

Compared with the old Ecodesign Directive, ESPR adds a large number of entirely new requirements:

1) Eco-design across the entire product life cycle

Companies must demonstrate product:

  • Durability

  • Repairability

  • Upgradability

  • Recyclability

  • Ease of disassembly

The EU’s aims:

Extend product lifetimes and reduce electronic waste

2) Carbon footprint and environmental impact

The following will gradually become mandatory:

  • Product carbon footprint calculation

  • Life cycle assessment (LCA)

  • Disclosure of environmental impact

Some products may be required to:

Publish carbon emissions data

3) Digital Product Passport (DPP)

One of the most important new mechanisms under ESPR:

Digital product passports will be created for all products

Contents include:

  • Material composition

  • Carbon footprint

  • Energy efficiency

  • Repair records

  • Compliance information

  • Serial-number traceability

Accessible via QR code or database.

This means the EU will build a transparency system covering the entire product life cycle

4) Repairability and spare-parts requirements

In future, products may be required to:

  • Provide repair manuals

  • Supply spare parts for 5–10 years

  • Have removable batteries

  • Use modular design

  • Not artificially restrict repair

This will have a major impact on electronic and medical equipment.

4. Implementation timeline (companies must watch closely)

Completed milestones

Date

Progress

2024

ESPR formally adopted

2025

Working plan published

2026

Rules for the first product groups begin

Expected implementation pace

2026–2027

First priority products:

  • Electronics

  • ICT equipment

  • Household appliances

  • Power supplies

  • Industrial equipment

2027–2029

Highly likely to be included:

  • Medical equipment

  • Laboratory equipment

IVD equipment

  • Imaging equipment

After 2030

Full coverage:

Almost all products entering the EU market

5. Impact on different types of companies

1) Medical device companies

Short term:

  • Not yet mandatory

  • But notified bodies (NB) have started paying attention

Medium term (3–5 years):

  • Carbon footprint requirements

  • Design for repairability

  • Spare-parts supply

  • Digital product passport

  • These will become new entry barriers.

2) Electronic equipment manufacturers

The biggest impact:

  • Energy efficiency

  • Standby power consumption

  • Repairability

  • Years of software support

  • Mandatory DPP

Many products will have to be structurally redesigned

3) Laboratory equipment companies

Highly likely to be in the first wave:

  • Analytical instruments

  • Scanning equipment

  • Testing equipment

Reasons:

High energy consumption, many electronic components and long life cycles

4) OEM/ODM factories

Will face:

  • Material traceability

  • Carbon footprint data

  • Supply chain disclosure

  • Design-for-repair requirements

Future EU requirements will:

Look not only at brand owners but also at manufacturers

6. What should companies do now?

Step 1: Check whether you will be in scope

We recommend that companies carry out:

An ESPR applicability pre-assessment

Assessing:

  • Product type

  • Whether it is electronic equipment

  • Length of life cycle

  • Energy consumption level

Step 2: Build eco-design thinking early

From the design stage, consider:

  • Structures that can be disassembled

  • Modularity

  • Repairability

  • Recyclable materials

  • Energy-efficiency optimisation

Otherwise, in future:

You are likely to have to redesign your products

Step 3: Prepare a digital compliance system

In future you will need to establish:

  • A materials database

  • Carbon footprint data

  • BOM (bill of materials) traceability

  • Life cycle data

These will become basic requirements for the EU market.

7. Conclusion: ESPR will be the next MDR-level regulation

For companies exporting to the EU:

The Ecodesign era is over, and the ESPR era has officially begun

The threshold for entering the EU market will be raised from:

single-product safety compliance to full life-cycle sustainability compliance

It is foreseeable that:

Within the next 5 years, ESPR will become as important as CE marking and the MDR

Companies that prepare early will gain a clear competitive advantage.

Want to know more?

If you would like to know whether ESPR affects your products, whether medical equipment will be included, how to build a compliance system in advance, or whether you need a digital product passport:

Everbiz is happy to share medical device expertise with industry clients. Please contact us for a professional assessment and consultation.

More articles:

Introduction to the ISO/IEC 27701 Standard

The Relationship Between ISO 27701 and Regulation (EU) 2016/679

Introduction to the GDPR (General Data Protection Regulation) for EU Medical Devices

EU Plans to Substantially Simplify the MDR: What Will Change for Certificates, Clinical Evidence and Notified Body Audits?

How Can Manufacturers Hedge Risk Through Insurance Under the MDR?

EVERBIZ Certification Services (Shanghai) Co., Ltd. (EVERBIZ) is a professional compliance service platform for testing, certification, consulting and training of medical products, dedicated to helping leading medical R&D companies at home and abroad improve their compliance capabilities and competitiveness. The company has offices and branches in Shanghai (China), Hong Kong, Munich (Germany), Salzburg (Austria) and Thailand, covering nearly 25 industries of compliance products (such as medical devices, new energy, household appliances, lighting, tools, laboratory instruments, machinery, in vitro diagnostics, wireless products and reagents).
Shanghai: Room 705, Building 6, Lane 111, Luxiang Road, Baoshan District, Shanghai | Germany: Landsberger Str. 155, 80687 München, Germany
Austria: Innsbrucker Bundesstraße 136/3, 5020 Salzburg, Austria
Hong Kong: Room A1, 11/F Winner Building, 36 Man Yue Street, Hung Hom, Kowloon, Hong Kong
Thailand: No. 850 Soi Lat Krabang 30/5, Lat Krabang Subdistrict, Bangkok 10520




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