EMC China Lab

Low Cost WEEE Compliance Registration Service

Views :
Update time : 2024-11-24

WEEE Overview

WEEE (Waste Electrical and Electronic Equipment) refers to the directive on the recycling of waste electrical and electronic equipment. Starting from August 13, 2005, producers of electrical and electronic equipment (EEE) in the EU market are legally required to bear the costs of recycling discarded products. Member states are obligated to establish their recycling plans and facilities, ensuring that end-users can conveniently and freely dispose of waste equipment.

 

Low Cost WEEE Compliance Registration Service(图1)


- WEEE in Germany 

Any seller distributing or having previously sold EEE in Germany must register for WEEE. Packaging, user manuals, and labels of the products must display the WEEE recycling symbol.

 

- WEEE in France 

France has implemented the WEEE directive into its national legislation as DEEE (Déchet d'équipement électrique et électronique). It specifies the recycling requirements for EEE sold in France.

 

WEEE is a mandatory regulation, and sellers must complete weee registration before placing products on the EU market. Compliance begins at the stage of product preparation for sale.

 

Frequently Asked Questions

What is WEEE Registration?

WEEE registration requires manufacturers of electronic products to take responsibility for the entire lifecycle of their products, including recycling after disposal. Electronic products sold in the EU, including on platforms like Amazon, AliExpress, and eBay, must be registered.

 

Which products require WEEE registration?

WEEE is categorized into six main groups:

1. Heat exchangers 

   Refrigerators, air conditioners, heat pumps, etc.

2. Display devices for private households 

   Monitors, TVs, tablets, etc.

3. Lamps/Glow-discharge lamps 

   Bulbs, fluorescent lamps, discharge lamps, etc.

4. Large electronic devices 

   Electronics with external dimensions exceeding 50 cm.

5. Small electrical and electronic devices 

   LED flashlights, Bluetooth thermometers, vacuum cleaners, etc.

6. Small IT and telecommunication devices 

   Cables, phones, routers, etc.

 

What is the most commonly registered WEEE category?

The Small Electrical and Electronic Devices category accounts for over 80% of registrations, including:

- LED strips, makeup mirrors, cameras, drones, etc.

 

What happens if WEEE is not registered?

1. E-commerce platforms may remove unregistered products.

2. Competitors may report violations, leading to potential product destruction and legal fees.

3. If detected by German authorities (Stiftung EAR or the Environmental Protection Association), penalties include:

   - Fines up to €100,000;

   - Confiscation of all profits in Germany;

   - A ban on product sales.

 

WEEE Registration Notes

1. Fees are calculated on an annual basis, so prepare for renewal early. 

2. Germany's WEEE compliance is frequently audited, but malicious store closures are rare. 

3. Avoid frequent changes to recycling partners, as modifications are costly and time-consuming. 

4. Do not confuse weee certification with registration; certification is separate and often misunderstood.

 

Documents Required for WEEE Registration in Germany

1. English and Chinese business license copies; 

2. Legal representative's ID (front and back); 

3. Product details (category, brand, dimensions) and images with logos; 

4. Amazon store information and product links; 

5. Contact email and phone number; 

6. German VAT number (optional but recommended).

 

Documents Required for WEEE Registration in France

1. Business license, legal representative, and store information; 

2. French WEEE application form (provided by China JJR platform); 

3. Registration delegation agreement (provided by China JJR platform).

 


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
What is the ISO 11607-1 Packaging Validation Test? What is the ISO 11607-1 Packaging Validation Test?
04 .25.2025
ISO 11607-1 ensures sterile medical packaging meets global safety standards. JJR Lab in China offers...
How to get an ISO 11737-1 Test Report? How to get an ISO 11737-1 Test Report?
04 .25.2025
Bioburden testing per EN ISO 11737-1 ensures medical device safety pre-sterilization. JJR Lab in Chi...
Orthopedic Implant Cleanliness Testing Orthopedic Implant Cleanliness Testing
04 .25.2025
Orthopedic implant cleanliness is key for biocompatibility and sterilization. China JJR Laboratory o...
What is ISO 10993-23:2021 Irritation Testing? What is ISO 10993-23:2021 Irritation Testing?
04 .25.2025
ISO 10993-23:2021 evaluates irritation risks of medical devices using in vitro/in vivo methods. JJR ...
ISO 10993-23 Irritation Testing Laboratory ISO 10993-23 Irritation Testing Laboratory
04 .25.2025
ISO 10993-23 irritation testing ensures device safety for skin, eyes, and mucosa. Professional testi...
EMI Emissions Testing EMI Emissions Testing
04 .25.2025
EMI emissions testing of electric/magnetic fields & disturbance power per CISPR standards. JJR L...
EMC Standards for Medical Devices EMC Standards for Medical Devices
04 .25.2025
EMC standards like IEC 60601-1-2 are vital for medical devices. China’s JJR Lab provides testing for...
What is FCC Class A vs. Class B? What is FCC Class A vs. Class B?
04 .25.2025
What is FCC Class A vs. B? Class A is for industrial use with looser limits; Class B suits homes wit...

Leave Your Message