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Savewo 3DMASK Vplus Disposable Medical Respirators – R Size (30 Pcs)

SGD $30.00

HSA Notified Class A Medical Device (License No: ES501633)

Package Contents:
  • 30 x individually packaged Savewo 3DMASK Vplus Disposable Medical Respirators
Size:
  1.  Regular Size
    • Unfolded (3D): 17(W) x 11.2(H) cm
    • Folded (flat): 20.8(W) x 8.1(H) cm
    • Fits more than 95% of adults
SKU: SAVEWO-3D3PC-VS-R-30 Categories: , , , Brand:
Product Features:
  • Designed and made in Hong Kong
  • Available in regular size
  • Stylish 3D design increases breathing space to ensure long-term wearing comfort
  • Innovative TypeCool+ filtration technology with ultra-high breathability
  • 24+ Hours Effective Filtration – Filtration efficiency maintains 99.9% effectiveness after 24 hours of exposure at 100% relative humidity
  • Latex-free and anti-allergic
  • ESPP Non-Woven Fabric – Smooth hydrophilic ESPP inner layer effectively maintains the ideal level of humidity inside the mask and prevents excessive loss of moisture from your skin
  • Manufactured with the safest colour pigments
  • Does not contain 212 types of Substance of Very High Concern (SVHC)
  • Does not contain azo dyes in textile
  • Does not contain fluorescein
  • Individual packaging
Certifications and Tests Passed:
  • Bacterial Filtration Efficiency (BFE) ≥ 99.9%
  • Particle Filtration Efficiency (PFE) ≥ 99.9% @0.1µm
  • Viral Filtration Efficiency (VFE) ≥ 99.9%
  • Fluid Resistance: Resists synthetic blood @ 160mmHg of pressure
  • Ultra-Low Breathing Resistance <2.4mmH2O @30L/min
  • Textile Flammability: Class I
  • Passed NIOSH 42 CFR 84 N95 (US) filtration and breathing resistance test
  • Conforms with ASTM F2100-19 Level 3 (US) / EN14683:2019 Type IIR (EU) / KMOEL-2017-64 KF94 (KR) / GB2626-2019 KN95 (CN) / JIS T 9001:2021 Class III (JP) (Tested by KAKEN)
  • Passed ISO10993-5 MEM Elution Test and ISO10993-10 Skin Irritation and Sensitisation Test, Biocompatibility of medical devices
  • ISO9001:2015 Quality Management System
  • ISO13485:2016 Medical Devices Quality Management System
  • ISO14001:2015 Environmental Management System
  • ISO14644-1:2015 Class 7 Cleanroom
  • Regulated by FDA (US), Registration Number: 3017178899
  • Regulated by MFDS (KFDA) (KR), Registration Number: 202107925
  • CE Marking Certification (EU)
  • Tested by Nelson Laboratories / KOTITI / STC

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