CE certification for mask protective clothing disinfectant

What is CE?
CE is a certification that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). The CE is the manufacturer's declaration that the product meets the requirements of the applicable EC directives. The CE marking is a symbol of free marketability in the European Economic Area (Internal Market).
Our Qualification and Certification:
9 Basic Modules required for CE Certification:
Module A: Internal Production Control
Module Aa: Intervention of a Notified Body
Module B: EC Type-examination
Module C: Conformity to Type
Module D: Production Quality Assurance
Module E: Product Quality Assurance
Module F: Product verification
Module G: Unit Verification
Module H: Full Quality Assurance
In reality the certification process consists of the following stages:
Stage 1: Identify the applicable Directive(s)
Stage 2: Identify the applicable requirements of the Directive(s)
Stage 3: Identify an appropriate route to conformity
Stage 4: Assessment of the product's conformity
Stage 5: Compile the technical documentation
1.Technical description
2.Drawings, circuit diagrams and photos
3.Bill of materials
4.Specification and, where applicable, EU declaration of conformity for the critical components and materials used
5.Details of any design calculations
6.Test reports and/or assessments
7.Instructions
8.EU declaration of conformity
Stage 6: Make a declaration and affix the CE marking
The requirements for the declaration vary slightly, but will at least include:
1.Name and address of the manufacturer
2.Details of the product (model, description and the serial number where applicable)
3.List of applicable sectoral Directives and standards that have been applied
4.A statement declaring that the product complies with all of the relevant requirements
5.Signature, name and position of the responsible person
6.The date that the declaration was signed
7.Details of the authorised representative within the EEA (where applicable)
8.Additional Directive/standard specific requirements
In all cases, except for the PPE Directive, all of the Directives can be declared on one declaration.
Product groups
The directives requiring CE affect the following product groups:
1. Active implantable medical devices (excludes surgical instruments)
2. Appliances burning gaseous fuels
3. Cableway installations designed to carry persons
4. Construction products according to Regulation (EU) No. 305/2011 under specific rules
5. Eco-design of energy related products
6. Electromagnetic compatibility
7. Equipment and protective systems intended for use in potentially explosive atmospheres
8. Explosives for civil uses
9. Hot-water boilers
10. In vitro diagnostic medical devices
11. Lifts
12. Low voltage
13. Machinery
14. Measuring Instruments
15. Medical devices
16. Noise emission in the environment
17. Non-automatic weighing instruments
18. Personal protective equipment
19. Pressure equipment
20. Pyrotechnics
21. Radio and telecommunications terminal equipment
22. Recreational craft
23. Restriction of the use of certain hazardous substances in electrical and electronic equipment RoHS 2
24. Safety of toys
25. Simple pressure vessels