By using this website, you agree to our privacy policy
×
Alpha Solway HX-2
P2 Disposable Fold-Flat Respirator
Alpha Solway HX-2
P2 Disposable Fold-Flat Respirator
Colour
Available Sizes
Features and Benefits
- Conforms to EN 149:2001+A1:2009 FFP2 NR
- Available in two size options, (regular - HX and large HXL) Ideal to fit a wide range of face shapes.
- Lightweight, fold flat respirator
- Flexible nose bridge
- Electrostatic filter media
- Tapered shape for enhanced fit
- Premium quality straps ensure stability on the face
- Non ferrous nose bridge
- Valve free
- Latex and silicone free
- Tested in accordance of EN14683:2019+AC:2019
Alpha Solway
Alpha Solway HX-2
The Alpha Solway HX-Series are horizontal fold flat disposable respirators designed to offer an excellent fit.
CE
Category III
Medical Device
⠀
Certification
EN 149:2001+A1:2009 FFP2 NR EN14683:2019 UK - Medical Device Directive (93/42/EEC & 2007/47/EC) EU - Medical Device Regulation (2017/745)
CE
Category III
Medical Device
⠀
Series
HX-Series
Outer Cover Material
Polypropylene
Filter Media Material
High Filtration Efficiency (Non-woven textile)
Inner Cover Material
Polypropylene
Headstrap Material
Textile Elastic
Nosebridge Material
Aluminium
Respirator Length (mm)
224
Respirator Width (mm)
96
Recommendations for use
This respirator is disposable and recommended for single shift use only. Do not attempt to clean or re-use.
EC compliance
Product conforms to the requirements of: UK Regulation 2016/425 on PPE, brought into UK Law and amended & Regulation (EU) 2016/425 of the European Parliament and of the Council as Personal Protective Equipment (PPE). Type-Examination, (Module B), Certi cates issued by: UK - CCQS UK Ltd., Level 2, 5 Harbour Exchange Square, London, E14 9GE, UK. [A.B. No. 1105]. EU - CCQS Certi cation Services Ltd., Block 1 Blanchardstown Corporate Park, Ballycoolin Road, Blanchardstown, Dublin D155 AKK1, Ireland. [N.B. No. 2834]. PPE is subject to the conformity assessment procedure, conformity to type based on Quality Assurances of the production process, (Module D), under the surveillance of the Approved/Noti ed Body(ies): UK - SGS UK Ltd., Rossmore Business Park, Ellesmere Port, Cheshire, CH65 3EN, UK. [A.B. No. 0120]. EU - SGS Fimko Oy, Takomtie 8, FI-00380, Helsinki, Finland. [N.B. No. 0598]. Class I UK - Medical Device Directive (93/42/EEC & 2007/47/EC) EU - Medical Device Regulation (2017/745).
