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A Place Of Discovery

Training in FIRST IIT KANPUR
N95 MASK

N95 FACE-MASK (CORONA VIRUS PROTECTION)

Bothered by dust, pollution and air-borne diseases? Breathe easier with SWASATM Anti-pollution face masks developed by E-Spin Nanotech Pvt Ltd. Featuring an innovative fibre membrane, SWASATM face masks pro- vide affordable and low-cost protection from all kinds of particulate con- taminants down to 2.5 um in size, including air-borne bacteria, pollen, fumes and other irritants. These masks have been tested and certified by CE mark and ISO mark to have a bacteria filtration efficiency of 99.9% as per standards. They feature a low pressure drop, making it easier to breathe through them. These masks are reusable, lightweight, comfortable, foldable and are easy to carry. They come with adjustable nose clips and a two-strap design to provide a custom fit with a secure seal that reduces the potential for eyewear fogging.

N99 MASK

Physical Properties

Testing Method

SWASA

Wight (GSM)

EN12127

160

Strength in longitudinal direction (N)

EN ISO 13934-1

200

Filtration Class

EN 779

F7

Bacterial filtration efficiency (%)

ASTM F2101-14

99.9 %

Efficiency of filtration PM 2.5 (%)

EN 779

-

Air permeability (l/m 2 /s)

EN ISO 9237

300 L/M 2 /S

Skin irritability

EN ISO 10993-1

NO RESPONSE

Bacterial Filtration Efficiency (BFE) & Differential Pressure (Delta P) Report

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 14683:2019, Annex B, and AS4381:2015.

The Delta P test is performed to determine the breathability of test articles by measuring the differential air pressure on either side of the test article using a manometer, at a constant flow rate. The Delta P test was designed to comply with EN 14683:2019, Annex C.

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.

For Booking Contact On

+91 818 184 5269 , +91 884 073 1350

Test Side

Nanofiber Side

BFE Test Area

~40 cm2

BFE Flow Rate

28.3 Liters per minute (L/min)

Delta P Flow Rate

8 (L/min)

Conditioning Parameters

85 ± 5% relative humidity (RH) and 21 ± 5°C for a minimum of 4 hours

Positive Control Average

3.3 X 10^ CFU

Negative Monitor Count

<1 CFU

MPS

3.1 pm

N95 MASK

For Booking Contact On

+91 818 184 5269 , +91 884 073 1350

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Download & View Certificate

Contact No. & Mail ID

Phone : +91 512 2504311

Mobile : +91 941 558 2516

Mail ID : inquiry@chaperonbiotech.com

Web Mail

Locations

CHAPERON BIOTECH PVT. LTD

PLOT. NO. 117/K71

SARVODAY NAGAR

KANPUR - 208 005

UTTAR PRADESH (INDIA)

CHAPERON BIOTECH PVT. LTD © 2013

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