bls-sge46-01- 1

Reusable BLS SGE46 Half Face Mask

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Category: Face Masks & Respirators Tags: face mask, facemask, half face mask, mask with filter, respiratory protection, reusable mask

Description
Additional information

Description

The BLS manufactured SGE46 Half Face Mask is reusable with changeable filters depending on the function you are wanting to use it for. The RD40 thread connection according to EN 148-1, universal among all respiratory protection devices.

The face piece is made of skin friendly silicone rubber , it is designed to universally adapt to all face sizes giving a better comfort and perfect fit.

The rigid body of the mask allows for even weight distribution of respirator, therefore it does not leave face marks, ideal for the user who may wear the equipment for long periods of time.

Face Piece: Silicone
Connection: EN148-1 (Universal)
Weight: 150g

Certification
Certified according with the European Regulation 425/2016 (Personal protective equipments)
Certified as PPE of III category, in presumption of conformity to harmonised standard EN 140:1998
Certified and controlled according to Annex D by Italcert S.r.l. (Notified Body n°0426)• CE marked
BLS management system is ISO 9001:2008 certified

Additional information

Size	M/L, S/M

Testimonials

We first ordered products from Hygiene UK at the start of the pandemic as our usual suppliers could not supply, and had increased their prices drastically. We were offered competitively priced and good quality PPE at a time when not many suppliers could. You delivered timely deliveries to all of my locations, and your team are always friendly and helpful. I will continue to work with you when required.

— Primera Healthcare

We've used Hygiene UK many times and have nothing but good things to say. Great Prices, reliable & quick delivery. We use Hygiene UK to supply our blue-chip clients so confidence is a must! Thoroughly recommend!

— Plane Talking

A vast range of PPE products at competitive prices, but crucially Hygiene UK's expertise behind the products, and the quality of them, is second-to-none.

— Broadbent Welding and Industrial Supplies

A great company to deal with, extremely reliable with a good range of products. Excellent product knowledge, great communication & customer service, fair prices and fast delivery.

— Jackson Handling

Hygiene UK is great business providing essential supplies to essential services.

— Hope City Foundation

Huge range of products at great prices. At a time of desperate need many were taking advantage of people, but not Hygiene UK. They have helped us and have been nothing but perfect. If you’re looking for masks, gloves, aprons, etc please give the team at Hygiene UK a call!

— Global Office Supplies

Pleasure to deal with, great communication and overall service levels. Highly recommended.

— Seldram Supplies

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FAQs

Find what you might need in our FAQ's...

What is an IVD medical device?

An IVD Medical Device is defined in the IVDR as “any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, piece of equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens derived from the human body.

What does in vitro diagnostic use mean?

In vitro diagnostics (IVDs) are tests that can detect disease, conditions and infections. In vitro simply means 'in glass', meaning these tests are typically conducted in test tubes, cassettes and similar equipment, as opposed to in vivo tests, which are conducted in the body itself.

What is In Vitro Diagnostic Regulation (IVDR)?

The IVDR is the new regulatory basis for placing on the market, making available and putting into service in vitro diagnostic medical devices on the European market. It will replace the EU’s current Directive on in vitro diagnostic medical devices (98/79/EC). As a European regulation, it will be effective in all EU member states and EFTA states immediately without need to be transferred into the law of respective states, however national laws may be adapted to back up some requirements in more detail.

When was the IVDR Implemented?

The IVDR came into force on 25 May 2017. Several implementing acts/guidance documents are being issued by the EU commission and are stipulated to complete some of the requirements to be met.

How can I contact you?

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