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Commodity code of protective clothing

Shanghai Sunland Industrial Co., Ltd is the top manufacturer of Personal Protect Equipment in China, with 20 years’experience. We are the Chinese government appointed manufacturer for government power,personal protection equipment , medical instruments,construction industry, etc. All the products get the CE, ANSI and related Industry Certificates. All our safety helmets use the top-quality raw material without any recycling material.

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Commodity code of protective clothing
Ce marking - Disposable products gloves and clothes ...
Ce marking - Disposable products gloves and clothes ...

It is commonly considered that all marketed products in the European Union must have the ,CE marking,.For sure, ,CE marking, is compulsory in products when their regulations establish it as a requirement.In this case, it must appear on the containers and packaging to show the user that the product follows the essential security and health criteria. . Nevertheless, not all products have to in

COVID-19: A guide to face masks - DentalNursing
COVID-19: A guide to face masks - DentalNursing

'Unfortunately, we (the European Safety Federation = trade association of suppliers of PPE) are informed by different sources about ‘certificates’ or other documents used as a basis for ,CE marking, of PPE (including FFP2/FFP3 ,masks, and eye protection), while these ‘certificates’ have no legal value and can not be used as conclusion of conformity assessment.

Classification Of Medical Devices And Their Routes To CE ...
Classification Of Medical Devices And Their Routes To CE ...

Table 1: ,CE marking, routes of Class I Medical Devices. Class IIa Medical Devices. Medical devices of class IIa could be such as surgical gloves, hearing aids, diagnostic ultrasound machines, etc. They usually constitute low to medium risk. Patients should use them for a short-term period, any less than 30 days.

Conditions for delivery and release of surgical face masks
Conditions for delivery and release of surgical face masks

Sterile surgical ,face masks, need to bear a ,CE marking, followed by a 4 -digit code. See also figure below. These 4 digits identify the notified body that assessed the elements for securing and maintaining the sterile conditions. The notified body issues a ,CE, certificate for this purpose.

CE self-certification for Class I device (face mask)
CE self-certification for Class I device (face mask)

14/7/2017, · Could you please provide me with any information regarding what's needed to do a self-certification for a ,CE mark, on a class I device (,face mask,)? I have checked with our NB and was told that a self-assessment can be done by us for the ,face mask,. Also, is the self-certification applicable for a class I sterile medical device? Appreciate all the ...

CE marking for masks face coverings and face shields used ...
CE marking for masks face coverings and face shields used ...

CE marking, a ,face, shield as a medical device is theoretically possible but there is no standard for this and in the absence of a widely agreed performance benchmark the rules for ,CE marking, medical devices, which require the manufacturer to have clear evidence that the device provides a medical benefit in response to one or more specific illness or disability, actually make it likely that it ...

Personal protective equipment directive - CE Marking assistant
Personal protective equipment directive - CE Marking assistant

Respiratory protective devices Full ,face masks, Requirements, testing, ,marking, EN 136:1998/AC:2003: EN 137:2006: Respiratory protective devices Self-contained open-circuit compressed air breathing apparatus with full ,face mask, Requirements, testing, ,marking, EN 138:1994

Guidance on regulatory requirements for medical face masks
Guidance on regulatory requirements for medical face masks

Medical ,Face Mask,: medical device ... ,CE,-marked and accompanied by the EC or EU declaration of conformity issued by the manufacturer. The manufacturer must prepare the appropriate technical documentation and keep it available for market surveillance authorities on request. The ,CE marking, should be affixed to the device where practicable and ...

COVID-19 what to do when importing PPE (e.g. FFP2 masks ...
COVID-19 what to do when importing PPE (e.g. FFP2 masks ...

remark : this article is valid for Personal Protective Equipment (PPE), such as protective ,masks, (type FFP2 or FFP3), protective glasses and ,face, shields, protective gloves and garments, etc. The rules for medical devices (e.g. medical or surgical ,masks,) are different and for those you should seek information from the relevant trade associations or authorities.

CE marking | Internal Market Industry Entrepreneurship ...
CE marking | Internal Market Industry Entrepreneurship ...

CE marking, is a part of the EU’s harmonisation legislation, which is mainly managed by Directorate-General for Internal market, Industry, Entrepreneurship and SMEs. The ,CE marking, for Restriction of Hazardous Substances is managed by Directorate-General for Environment .

Use of face masks designated KN95
Use of face masks designated KN95

KN95 ,face mask,. KN95 is a ... For those that are ,CE, marked, suppliers must be able to demonstrate how they know the documentation and ,CE marking, is genuine, supported by Notified Body documentation showing compliance with the essential health and safety requirements as required by the Personal Protective Equipment Regulations (EU) 2016/425.

Do my products need CE marking? Find the answer in this post.
Do my products need CE marking? Find the answer in this post.

The ,CE marking, applies to products placed in the market or put into service in the European Economic Area. Even so, it only it applies only for certain product groups or product aspects, as we will see in the next step. To answer the question whether a product needs to be ,CE, marked, ...

Recommendation to allow protective equipment without CE ...
Recommendation to allow protective equipment without CE ...

These items must follow the NEN standard. Due to the high demand within the EU for personal protective equipment, there is a recommendation that under specific circumstances some medical devices (e.g. ,face masks, used for medical purpose) may be made available on the Union market, even if they do not yet bear the ,CE mark,.

COVID-19: A guide to face masks
COVID-19: A guide to face masks

‘Unfortunately, we (the European Safety Federation = trade association of suppliers of PPE) are informed by different sources about ‘certificates’ or other documents used as a basis for ,CE marking, of PPE (including FFP2/FFP3 ,masks, and eye protection), while these ‘certificates’ have no legal value and can not be used as conclusion of conformity assessment.

CE marking for masks face coverings and face shields used ...
CE marking for masks face coverings and face shields used ...

CE marking, a ,face, shield as a medical device is theoretically possible but there is no standard for this and in the absence of a widely agreed performance benchmark the rules for ,CE marking, medical devices, which require the manufacturer to have clear evidence that the device provides a medical benefit in response to one or more specific illness or disability, actually make it likely that it ...

How to identify suspicious fake or misleading marks ...
How to identify suspicious fake or misleading marks ...

This is a Jusenyuan respirator that looks like a typical earloop KN95 respirator ,mask,. The seal on the ,mask, has an FDA logo (illegal), FFP2 (no proof), N95 (no proof) and ,CE, EN149:2001+A1:2009 ...

Conditions for delivery and release of surgical face masks
Conditions for delivery and release of surgical face masks

Sterile surgical ,face masks, need to bear a ,CE marking, followed by a 4 -digit code. See also figure below. These 4 digits identify the notified body that assessed the elements for securing and maintaining the sterile conditions. The notified body issues a ,CE, certificate for this purpose.