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TopiVac Clinic V4 Type Professional Hybrid Topical Wound Treatment Device and Dressing; are an active hybrid system that applies controlled local negative pressure that supports healing in noninvasive acute, infected and chronic wounds and irrigates the wound centre with topical fluids. It increases the life quality of the patient and reduces the treatment costs. It heals wounds faster and more effectively than conventional vacuum assisted devices on the market. It enables clinical studies for physicians.
TopiVac Wound Care Device is a non-invasive wound treatment method developed by TEKNOMAR, which has proven itself in wound healing. This treatment unit is needed to apply topical hybrid treatment methods to the wounded area.
Vacuum Assisted Therapy T-NPWT - Conventional vacuum assisted therapy standard negative pressure wound dressing; It is an active system that supports healing in non-invasive acute and chronic wounds and applies controlled local negative pressure. It is known that the negative pressure wound closure system accelerates tissue healing by increasing microcapillary circulation, but cannot prevent the development of infection in a closed environment and does not provide enough removal of necrotic material.
Vacuum Assisted Therapy & Wound Irrigation - Conventional vacuum assisted therapy + oxygenated water, ozonized water or bidistillated water
Gas Therapy - Oxygen (O2) or Ozone (O3) Gas
Vacuum Assisted Therapy & Gas Therapy (O2 / O3) - Conventional vacuum assisted therapy + Oxygen (O2) or Ozone (O3) Gas
Vacuum Assisted Therapy & Gas Therapy (O2 / O3) & Wound Irrigation - Conventional vacuum assisted therapy + Oxygen (O2) or Ozone (O3) Gas + Oxygenated water, ozonized water or bidistillated water
Electrotherapy (E.Tens) - Supporting pain treatment and wound healing with electrostimulation, providing polarization in granilization.
Yes, with MDA. MDA is the government agency entrusted to serve the Malaysia medical device’s industry. It is a federal statutory agency under the Ministry of Health Malaysia to implement and enforce and to address public health and safety issues related to medical devices and to facilitate medical devcie trade and industry.
MEDICAL DEVICE REGISTRATION CERTIFICATE Section 5(1) of Act 737
Registration No.: GC4602024-190236
Registration Validity Date: 25/11/2024 - 24/11/2029
Yes, you can find the related pdf files below
You can click the link below about the Topivac V4 product