BURN CARE AND WOUND CARE MARKET ANALYSIS

Burn Care and Wound Care Market, by Product Type (Topical Agents {Antibiotics, Antiseptic, Antifungal, and Others {Chlorhexidine, among others}}, Wound Therapy Device {Negative Pressure Therapy Device, Hyperbaric Oxygen Equipment, Pressure Relief Devices, and Others {Electrical Stimulation Devices}}, Surgical Wound Care Products {Sutures, Staplers, and Others {Tissue Adhesives, Sealants and Glues}}, Skin Grafts {Split-thickness Grafts, Full-thickness Grafts, and Composite Grafts}, and Advanced Dressing {Foam Dressing, Collagen Dressing, Hydrogel Dressing, and Others {Hydrocolloid, Alginate, among others}}, and Traditional Burn Care {Medical Tapes, Dressings, and Cleansing Agents}), by Application (Burn Degree {First Degree, Second Degree, Third Degree, and Fourth Degree}, and Wound Type (Surgical Wounds, Ulcers {Pressure Ulcers, Diabetic Foot Ulcers, and Arterial and Venous Ulcers}, Traumatic Wounds, and Others {Microbial Infection, among others})), by End User (Hospitals and Clinics, Burn Care Centers, and Others {Home Care, among others}), and by Region (North America, Latin America, Europe, Asia Pacific, Middle East, and Africa) - Size, Share, Outlook, and Opportunity Analysis, 2022 - 2030

Published In : Nov 2022
Code : CMI4836
Pages :180
Formats :
Excel and PDF
Industry : Medical Devices

Market Challenges And Opportunities

Global Burn Care and Wound Care Market - Restraint

Product recalls are the factors that are expected to hinder growth of the global burn care and wound care market over the forecast period.

For instance, in June 2021, Smith & Nephew, a global medical equipment manufacturing company, recalled its Jelonet 5 X 5 contact layer paraffin dressing carton post discovery of a potential breach in the sterile barrier and paraffin leakage.

Moreover, in March 2018, Integra LifeSciences, a U.S.-based medical device company recalled its Manuka Honey Wound Gel, which is used for wound healing of minor scalds and burns, minor cuts, lacerations, and minor abrasions. The reason for recall was incorrect gel part number listed in a master manufacturing record. The product was finally terminated in July 2018.