Wound Dressings & Bandages Suppliers & Bulk Manufacturers
Available Forms: Adhesive dressings, Non-adhesive dressings, Bandages
Available Strengths: Various sizes, material types, and absorption capacities, suitable for acute and chronic wounds
Reference Brands: 3M, Smith & Nephew, Hollister, Mepilex, Tegaderm
Category:
Medical Devices
Wound dressings and bandages protect wounds, absorb exudates, and maintain a moist healing environment. They prevent infection, promote faster healing, and reduce scarring. Benefits include infection control, pain reduction, and supporting optimal wound healing, ensuring effective care in medical and veterinary practices.
Wound dressings & bandages is available in Adhesive dressings, Non-adhesive dressings, Bandages
and strengths such as Various sizes, material types, and absorption capacities, suitable for acute and chronic wounds.
Sourced from GMP-certified and ISO-compliant manufacturers, this API meets
global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical
formulation and commercial manufacturing, Wound dressings & bandages is supplied in
bulk quantities with complete regulatory support including DMF, COA, and MSDS.
|
Technical Specifications & Supply Details
|
| Lead Time |
7 to 60 days (depending on batch size & schedule) |
| MOQ |
As per manufacturer’s batch size |
| COA |
Available with every batch |
| Regulatory Dossier / DMF |
Available upon request |
| Export Documentation |
FSC, COA, Manufacturing License, Product Permission |
| Standards |
IP, BP, USP |
| Certifications |
WHO-GMP, EU-GMP, USFDA (as applicable) |
Wound dressings & bandages can be exported to over 30 countries across Asia, Africa, Europe,
and Latin America. Flexible packaging, competitive pricing, and a verified supplier
network make Pharmatradz a trusted sourcing partner for pharmaceutical companies
and contract manufacturers worldwide.
Product Description:
Wound dressings and bandages in the EU and US are regulated to ensure safety, efficacy, and quality. In the US, FDA approval involves clinical validation, safety assessments, and GMP compliance. In the EU, CE marking certifies conformity with the Medical Device Regulation (MDR). These products undergo validation, stability testing, and audits, with detailed documentation including safety profiles, clinical data, and manufacturing practices. For licensing procedures, approved dossiers, and the latest regulatory updates, visit Pharmatradz. Ensuring compliance guarantees access to reliable, effective wound care products essential for infection control and optimal healing worldwide, supporting healthcare and veterinary rehabilitation efforts.
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