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BFE99% Non Woven Disposable Face Mask green Color with inner spot earloop
Product Details:
| Place of Origin: | China |
| Brand Name: | Delta-Medi |
| Certification: | CE ISO |
| Model Number: | DM-780085 |
Payment & Shipping Terms:
| Minimum Order Quantity: | 200000pcs |
|---|---|
| Price: | negotiable |
| Packaging Details: | 50pcs-box ,2000Pcs/Carton 50X40X40cm |
| Delivery Time: | 10-20days |
| Payment Terms: | T/T, Western Union, MoneyGram |
| Supply Ability: | 1000000PCS Per Day |
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Detail Information |
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| Material: | SBPP+filter Paper+SBPP/SMS | Instrument Classification: | Class I |
|---|---|---|---|
| Color: | Blue,Green,Dark Blue,white,pink | Style: | Tie On Or Ear-loop |
| Sterilization: | ETO/ NO ETO | Pack Count: | 50/2000 CTN |
| Size: | 17.5x9.5cm | Layer: | 3ply / 4ply |
Product Description
BFE>99%Disposable Face Mask
Tech Standard & Specifications
1. BFE>99%.
2. Style: tie-on/ear-loop
3. Fluid resistant layer with unique single pleated design to prevent fluid pooling.
4. Skin irritation:The material of face mask is soft, without odor and without skin irritation.
5. Nose bar:The nose bar is metal band, which can be bended easily and adapt to the contour of the nose.
6. Function:The face mask is applicable to the doctor and patient, it can prevent blood, body fluids and splash objects.
Size Chart
| Tape | Measurement |
| Adult | 17.5x9.5cm |
| Child | 14.5x9.5cm |
The BFE test is performed to determine the filtration efficiency of test articles by comparing
the bacterial control counts upstream of the test article to the bacterial counts downstream. A suspension
of Staphylococcus aureus was aerosolized using a nebulizer and delivered to the test article at a constant
flow rate and fixed air pressure. The challenge delivery was maintained at 1.7 - 2.7 x 10^ colony forming
units (CFU) with a mean particle size (MPS) of 3.0 ± 0.3 pm. The aerosols were drawn through a six-
stage, viable particle, Andersen sampler for collection. This test method complies with ASTM F2101-14,
EN 14683:2014, Annex B, and AS4381:2015.
All test method acceptance criteria were met. Testing was performed in compliance with US FDA good
manufacturing practice (GMP) regulations 21 CFR Parts 210, 211 and 820
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