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.
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
How Can Manufacturers Hedge Risk Through Insurance Under the MDR?