Laboratoires Urgo S.A.

Web: http://www.urgo.fr
Address: 42 rue de Longvic, Chenove Cedex 21000, France
Phone: +33-(380)-54.50.00 | Fax: +33-(380)-44.74.52 | Map/Directions >>

Profile: Laboratoires Urgo S.A. specializes in research and development, and production & clinical research to demonstrate the effectiveness of therapeutic products. We manufacture surgical adhesive dressings for wound healing. Our brands include Urgo®, Humex® and Alvityl®. Our Urgo is a range of liquid bandages. We develop advanced medical solutions, and support different problems of prevention and treatment of wounds and damaged tissues. We also provide Humex reflex defense nasal spray. It helps to prevent the common cold, and influenza A H1N1. The nasal spray acts not only against the virus in the nasal cavity, but also against the invasion of new viruses. They are trapped by a barrier formed by the active renewal applications.

FDA Registration Number: 9615662
US Agent: Ann Marie Hettinger / Hollister, Inc.
Phone: +1-(847)-680-2128 Fax: +1-(847)-680-3981 E-Mail:

4 Products/Services (Click for related suppliers)

• Drug Wound Dressing (FDA Code: FRO)

• Hydrophilic Wound Dressings (FDA Code: NAC / 878.4018)

A hydrophilic wound dressing is a sterile or non-sterile device intended to cover a wound and to absorb exudate. It consists of nonresorbable materials with hydrophilic properties that are capable of absorbing exudate (e.g., cotton, cotton derivatives, alginates, dextran, and rayon). This classification does not include a hydrophilic wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.

• Occlusive Wound and Burn Dressing (FDA Code: MGP)

• Occlusive Wound Dressing (FDA Code: NAD / 878.4020)

An occlusive wound dressing is a nonresorbable, sterile or non-sterile device intended to cover a wound, to provide or support a moist wound environment, and to allow the exchange of gases such as oxygen and water vapor through the device. It consists of a piece of synthetic polymeric material, such as polyurethane, with or without an adhesive backing. This classification does not include an occlusive wound dressing that contains added drugs such as antimicrobial agents, added biologics such as growth factors, or is composed of materials derived from animal sources.