CE Marking on ecological vacuums

G

gpegg

#1
Hello, I am a student and have a project on how can we add CE marking on ecological vacuums.

As I have seen the vaccum must comply with directives:
1) 2006/95/ec low voltage directive
2) 2004/108/ec Electromagnetic compatibility
3) 2009/125/ec European Ecodesign Directive
4) 2005/32/ec Ecodesign for energy-using appliances
5) 2010/30/eu on the indication by labelling and standard product information of the consumption of energy and other resources by energy-related products

and regulations:
1) 666/2013 eco-design requirements
2) 665/2013 labeling requirements

To ad the CE mark are directives 1,2 and 3 enough or do I have to mention all directives and regulations?
 
Elsmar Forum Sponsor

Ronen E

Problem Solver
Staff member
Moderator
#2
Hello, I am a student and have a project on how can we add CE marking on ecological vacuums.

As I have seen the vaccum must comply with directives:
1) 2006/95/ec low voltage directive
2) 2004/108/ec Electromagnetic compatibility
3) 2009/125/ec European Ecodesign Directive
4) 2005/32/ec Ecodesign for energy-using appliances
5) 2010/30/eu on the indication by labelling and standard product information of the consumption of energy and other resources by energy-related products

and regulations:
1) 666/2013 eco-design requirements
2) 665/2013 labeling requirements

To ad the CE mark are directives 1,2 and 3 enough or do I have to mention all directives and regulations?
Hello and welcome to the Cove :bigwave:

Strictly discussing CE marking (not necessarily all legal requirements for placing on the EU market), only the directive you listed as #1, 2 & 3 provide for CE marking directly.

Please note:
1. Responsibly stating whether those 3 directlives actually apply to the subject product requires access to the full details and a careful examination (I guess that that's your job as the student carrying out the task ;)).
2. Other directives that provide for CE marking may be applicable - careful examination required.
3. Other legal instruments may indirectly apply (via reference), either included in your list or otherwise.

Determining the regulatory scope for CE marking of a product is not a 5 minute job, and is case specific. I guess that unless a good fairy shows up, you'll have to do your best, submit and see what feedback you get from your professor.

Cheers,
Ronen.
 
Last edited:
G

gpegg

#3
Hello and welcome to the Cove :bigwave:

Strictly discussing CE marking (not necessarily all legal requirements for placing on the EU market), only the directive you listed as #1, 2 & 3 provide for CE marking directly.
Thank you Ronen! You were very helpful!
That's what I also thought, but I was not really sure. I'll study the directives very carefully to be sure about the procedure.
 
G

gpegg

#5
You may also want to look at 2011/65/EU, RoHS Directive to check whether your product is in scope.
I looked at RoHS Directive and think that dust vaccums are not in scope.
I am not sure about R&TTE Directive (2014/53/EU)... as I found a Declaration of Conformity of a vacuum that mentions that the product is in compliance with this directive and can't figure out why.
 

Attachments

Last edited by a moderator:

CharlieUK

Quite Involved in Discussions
#6
The RoHS Directive applies to any electrical/electronic device unless it falls under a specific exemption, and I don't see any that you could apply.

The Samsung machine appears to have a wireless sensor, which is why R&TTE has been applied - if you don't have one, you wouldn't apply R&TTE as you have stated,

Charlie
 
Last edited:
Thread starter Similar threads Forum Replies Date
Z Is IQ necessary for laser marking validation? EU Medical Device Regulations 3
A Is it mandatory to obtain ISO13485 certificate prior to CE marking? EU Medical Device Regulations 8
G CE marking of MD and IVD set EU Medical Device Regulations 3
M CE marking for NON-EU EU Medical Device Regulations 0
NDesouza Getting Rid of Part Marking Errors Benchmarking 39
S CE marking for a product upgrade CE Marking (Conformité Européene) / CB Scheme 0
P CE Marking UK Membership CE Marking (Conformité Européene) / CB Scheme 1
J Powered wheelchairs (Class IIa) in the process of CE marking and use in hospitals CE Marking (Conformité Européene) / CB Scheme 4
D CE Marking Requirements MDD & MDR - new product development covered under same scope EU Medical Device Regulations 1
N CE marking colour for Medical Devices CE Marking (Conformité Européene) / CB Scheme 4
A EAC Marking in Medical Device Other Medical Device Regulations World-Wide 0
B Marking of Medical Electrical equipment and accessories - Cl. 7.2.2 "Identification" and Cl. 7.2.4 "Accessories" IEC 60601 - Medical Electrical Equipment Safety Standards Series 4
M Clinical investigations of medical devices - not for CE marking EU Medical Device Regulations 0
P Marking Machinery for Israel CE Marking (Conformité Européene) / CB Scheme 3
K Does company who manufacture but does not design or carry out clinical trials is responsible for CE marking for single use medical devices? ISO 13485:2016 - Medical Device Quality Management Systems 3
M Does cFDA accepts FDA approval or CE marking? China Medical Device Regulations 1
I Reducing CE marking cost using manufacturer test reports CE Marking (Conformité Européene) / CB Scheme 5
C CE marking for general IVD (self-certified) & ISO 13485 QMS requirements - auditing EU Medical Device Regulations 6
Ed Panek Is Shelf Life Change a significant change? CE Marking CE Marking (Conformité Européene) / CB Scheme 7
CPhelan Using clinical trial safety data for evidence for CE marking EU Medical Device Regulations 7
N How to Write and Compile a Technical File for CE Marking CE Marking (Conformité Européene) / CB Scheme 4
CPhelan Do you require MDSAP for CE Marking of a Medical Device or is ISO13485:2016 with clinical data sufficient? CE Marking (Conformité Européene) / CB Scheme 5
P CE Marking EN ISO 13849-1: Electrical Panel behind interlocked doors CE Marking (Conformité Européene) / CB Scheme 9
M Cleaning Process after laser marking on orthopaedic implants Other Medical Device and Orthopedic Related Topics 3
H Safety and efficacy study for CE marking CE Marking (Conformité Européene) / CB Scheme 1
S Difficulty Finding A Notified Body for CE Marking - No Capacity Registrars and Notified Bodies 5
Kuldeep Singh Post Market Clinical Follow up and CE Marking for Class IIb medical X-Ray products CE Marking (Conformité Européene) / CB Scheme 1
J CE Marking for vibrator personal pleasure toy CE Marking (Conformité Européene) / CB Scheme 16
JoshuaFroud CE Marking and Brexit - Product shipped to a distributor prior to the March deadline EU Medical Device Regulations 2
M Informational Design for new product safety marking for the no-deal Brexit scenario Medical Device and FDA Regulations and Standards News 1
E Safety work instruction if the equipment have the CE Marking and a Manual with safety instruction Various Other Specifications, Standards, and related Requirements 16
Z Direct Part Marking (DPM) requirements for Class II Medical Devices Manufacturing and Related Processes 0
M Medical Device News FDA Guidance - UDI: Policy Regarding Compliance Dates for Class I and Unclassified Devices and Certain Devices Requiring Direct Marking Other US Medical Device Regulations 0
J Virtual Manufacturer and CE Marking EU Medical Device Regulations 8
N CE marking for distributed product CE Marking (Conformité Européene) / CB Scheme 1
S CE Marking requirements - A Medical device with different config sold under same name EU Medical Device Regulations 0
J Class 1 CE Marking - Can this be removed from the label on the product? CE Marking (Conformité Européene) / CB Scheme 4
I Tool Control Marking Voiding Warranty AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
C Data Matrix and DPM (direct part marking) UDI Standards - ISO/IEC TR 29158 Other US Medical Device Regulations 2
K UDI Direct Marking Compliance Date Clarification and one other UDI question Other US Medical Device Regulations 0
T CE Marking & Compliance to MDD, EMC, RoHS, and GPSD REACH and RoHS Conversations 4
J Installation Qualification (IQ) and Operational Qualification (OQ) for Laser Marking 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
N How to obtain Own Brand Label (OBL) CE Marking? EU Medical Device Regulations 18
Q Does CE Marking include compliance to WEEE and packaging waste? CE Marking (Conformité Européene) / CB Scheme 4
C Looking for Testing Laboratory for Aluminum Products - CE Marking General Measurement Device and Calibration Topics 5
J CE Marking Requirements and IEC 60617 - Electrical Schematics Symbols CE Marking (Conformité Européene) / CB Scheme 1
H CE Marking on Multiple-Components Medical Products EU Medical Device Regulations 8
U CE Marking of Customized Ruggedised Computer Systems Solutions CE Marking (Conformité Européene) / CB Scheme 5
L IEC/EN 60601-1 Certificate required before CE Marking? IEC 60601 - Medical Electrical Equipment Safety Standards Series 3
L Canada Electrical Equipment Marking Language Requirements IEC 60601 - Medical Electrical Equipment Safety Standards Series 2

Similar threads

Top Bottom