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Gray Flat Disposable Medical Face Masks , Disposable Dust Mask 5 Years Expiry Date

Xiantao Xincheng Plastic Products Co.,Ltd
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Xiantao Xincheng Plastic Products Co.,Ltd

Gray Flat Disposable Medical Face Masks , Disposable Dust Mask 5 Years Expiry Date

Country/Region china
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Product Details

FFP2V Vertical Foldable Mask ,Fold Flat Mask ,CE Standard Facial Disposable

 

1 . Descriptions 

 

MX-5006 FFP2V Dust Mask with 4-ply non-woven/elasticated strap ,fold flat dust mask ,convenience take/packing: neutral color box, also can OEM/disposable dust mask with valve/protect against dust and liquid.The mask is light and comfortable. The internal nosepiece is made of velvet/sponge double-layer. There are no exposed metal components; the external nosepiece used to adjust the mask on the face is metal coated. Structure and materials are long lasting and avoid the collapse in humid environments.

 

 

2. Advantages

 

COMFORTABLE&SOFT
4 layers virgin non woven fabric,45g hot air makes mask soft and puffy ,comfortable to touch skin, carbon layer is anti odors.

 

3D MODEL L ING
Three- Dimentional,imitate the shape of nose and mouth,perfectly wrapping people's mouth and nose.

 

THE VALVE'S WORKING PRINCIPLE
it is close when inhale,so outside particles couldn't flow in.It is open when exhale to wipe out the air emissions and help breath easily.

 

NOSE CLIP&NOSE FOAM
Nose foam prevents leakage and provide twice protection. Nose foam is made of sponge.It is comfortable to settle nose foam on nose bridge.

 

 

3. Packing

 

The package of this fold mask with is 12pcs/box , 20box/carton.

 

4 . Certification

 

This product has been tested according to the following European Standard:

  • EN149: 2001 +A1: 2009. Respiratory protective devices. Filtering half masks to protect against particles. Requirements, testing, marking.It complies with European Regulation (EU) 2016/425 on Personal Protective Equipment (PPE).Category III.
  • EU type examination certificate (module B) issued by BSI , notified body n°0086.The PPE is subject to the conformity assessment procedure based on internal production control plus supervised product checks at random intervals set out in Annex VII under surveillance of BSI , notified body n°0086.

 

 

 

 

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