Alpha Solway - Model 3530 -P3 Disposable Pre-Formed Cup-Shaped Respirator

• Conforms to EN 149:2001+A1:2009 FFP3 NR and EN 14683:2019+AC:2019
• Four-point head strap adjustment and preformed nose bridge improves the fit and removes the need for regular adjustment
• Available in two size options, (regular and small). Ideal to fit a wide range of face shapes
• PVC Foam Inner Face Seal and soft touch elastic for maximum comfort
• Protection option: FFP3
• Also available in valved

• Notified Body: CE0598
• Certification: EN 149:2001+A1:2009 FFP3 NR and EN 14683:2019+AC:2019
• CE: Category III
• Medical Device
• Series: 3500 Series
• Outer Cover Material: Polypropylene
• Filter Media Material: Melt Blown PP Spunbond PP and PE
• Inner Cover Material: Polyester
• Headstrap Material: PA Woven Elastic (Latex-Free Rubber)
• Nosefoam Material: PVC Foam
• Respirator Length (mm): 150
• Nosebridge Length (mm): 45
• Headband length (mm): 420
• Headband clip Length (mm): 37
• Respirator Width (mm): 54
• Nosebridge Width (mm): 40
• Headband Width(mm): 14
• Headband clip width (mm): 19
• Respirator Height (mm): 130
• Nosebridge Height (mm): 35
• Headband Height(mm): 0.4
• Headband clip height (mm): 4
• 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 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/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).