CE-Marking Quotation Request

Submitted by maaz on May 3, 2023 - 8:01am
 
1 Start 2 Complete
Please provide your firm's legal name.
Where project needs to be implemented
Estiamted man power including contractor staff and permenant employees.
Your role in business supply chain.
What is/are the name(s) of the product(s)? What is/are the Intended Purpose(s) of the product(s)? How long has the product been placed on your domestic market? What is the estimated retail unit price in USD? (Use ENTER key to break lines)
Applicable stadnards identified applicable to your products
Please choose your product group.
Only Applicabe to MD product group
Only fill the below field if your product belongs to their group.
i.e., a kind of instrument, apparatus, appliance, material or other article, whether used alone or in combination, including the software necessary for the proper application, intended by the manufacturer to be used for human beings for the purpose of: diagnosis, prevention, monitoring, treatment or alleviation of a disease, an injury or a handicap. investigation, replacement or modification of the anatomy or of a physiological process. control of conception and which does not achieve its principal intended action in or on the human body by pharmacological, immunological or metabolic means, but which may be assisted by such means 
Only Applicabe to IVD product group
Only fill the below field if your product belongs to their group.
which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, equipment, or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens, including blood and tissue donations, derived from the human body, solely or principally for the purpose of providing information: - concerning a physiological or pathological state, or - concerning a congenital abnormality, or - to determine the safety and compatibility with potential recipients, or - to monitor therapeutic measures ?*
Documents Available
For each product applying for ceritification following documents are required
YesNo
Technical description
Bill of Material
Drawing, cricuit diagrams and photo
Details of design calculations
Risk Assessment /FMEA
Work Instructions
Labeling and Packaging Sample
Specification Declaration of Conformance for components and material if used
Test reports and assessments
EC Declaration of Conformity
Documents available of each product
for multiple select use control key.
Do you require certification quotes with consulting charges?
Files must be less than 1 MB.
Allowed file types: jpg jpeg png pdf.