World leading Wellkang Tech Consulting group offer EU/EC European authorised/authorized representative & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
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Wellkang Ltd
CE-marking.com CE-marking.eu
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Wellkang Ltd
CE-marking.com CEmarking.org
29 Ha●●●●●treet
LO●●ON , England, W1G 9QR
GB
View this contact
Wellkang Ltd
CE-marking.com CE-marking.org
29 Ha●●●●●treet
LO●●ON , England, W1G 9QR
GB
View this contact
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EC Rep: EU/EC European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services | eaar.org Reviews
https://eaar.org
World leading Wellkang Tech Consulting group offer EU/EC European authorised/authorized representative & CE Mark (CE Marking) consulting services for medical devices MDD, low voltage electrical equipment LVD, cosmetics, EMC, PPE.
eaar.org
Guide on Class I (Is/Im) MDD- Medical Devices CE marking (mark) & European (EU) Authorized Representative service
http://www.eaar.org/medical-devices-class-i.html
As of 21 March 2010. EEA European Authorised/Authorized Representative. Must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EEA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. Steps for Class I medical devices compliance. Classification: ensure the device is a Class I medical device. Compile the Technical File. Once the manufact...
Online Shop of Wellkang: Accepting Credit Card/Check/Money Order/Bank Transfer/Internet Banking
http://www.eaar.org/order-now.html
Guide on Class IIb MDD- Medical Devices CE marking (mark) & European (EU) Authorized Representative service
http://www.eaar.org/medical-devices-class-IIb.html
As of 21 March 2010. EEA European Authorised/Authorized Representative. Must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EEA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. Steps for Class IIb medical devices compliance. Classification: ensure the device is a Class IIb medical device. Compile the Technical File. Ii) the proce...
Why choose Wellkang? Unique benefits of choosing Wellkang as European (EEA/EU) Authorised/Authorized Representative!
http://www.eaar.org/authorised-representative/why-choose-wellkang-your-benefits-by-appointing-wellkang-as-your-eu-authorized-representative.html
As of 21 March 2010. EEA/EU/EC European Authorised/Authorized Representative. Must be designated by a non-EEA manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EEA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. Be your European Authorised/Authorized Representative! Why do you need a European Authorised/Authorized Representative? How can Wellkang help you?
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EC Rep: EU/EC European Authorised Representative/Authorized Representative & CE Mark (CE Marking) consulting services
As of 21 March 2010. EU/EC European Authorised/Authorized Representative. Must be designated by a non-EU manufacturer of medical devices as required by directive 2007/47/EC, are you ready? Medical Devices and IVD. In Vitro Diagnostic Medical. Other EU/EFTA authorities by world-leading CE Marking. Specialists based in London/UK. Click here to get FREE Guide. You export to Europe? UL mark; China Compulsory Certification- CCC Mark. China RoHS compliance and solutions, etc. How can Wellkang help you? Wellkan...
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