By using this website, you agree to our privacy policy
×
ALPHASOL+ AP-3
P3 Vertical Fold-Flat Respirator
ALPHASOL+ AP-3
P3 Vertical Fold-Flat Respirator
Colour
Available Sizes
Features and Benefits
- Conforms to EN 149:2001+A1:2009 FFP3 NR & EN14683:2019+AC:2019
- Lightweight, vertical fold flat respirator
- Flexible nose bridge
- Electrostatic filter media
- Inner seal around the nose area for an effective fit
- Available in two size options (AP-3 – Regular, APS-3 – Small).
- Ideal to fit a wide range of face shapes
- Splash Resistant
- Latex Free
- Adjustable loop through straps
- Non Ferrous
Alpha Solway
ALPHASOL+ AP-3
The Alphasol+ is a vertical fold flat disposable respirator designed with an inner face seal to offer an excellent fit for all face shapes.
CE
Category III
Medical Device
⠀
Certification
EN 149:2001+A1:2009 FFP3 NR | EN 14683:2019+AC:2019
CE
Category III
Medical Device
⠀
Series
AlphaSOL+
Outer Cover Material
Polypropylene
Filter Media Material
High Filtration Efficiency (Non-woven textile)
Inner Cover Material
Polypropylene
Headstrap Material
Textile Elastic 64% Polyester / 36% Elastane (Latex Free)
Nosefoam Material
Polyethylene
Nosebridge Material
Aluminium
Respirator Length (mm)
160
Respirator Width (mm)
125
Respirator Height (mm)
10
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 requirement 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), Certificates issued by: UK - CCQS UK Ltd., Level 2, 5 Harbour Exchange Square, London, E14 9GE, UK [A.B. No. 1105]. EU - CCQS Certification Services Limited, 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 Assurance of the production process, (Module D), under the surveillance of the Approved/Notified 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).
