Integra® Dermal Regeneration Template
Limit uncertainty with Integra® DRT, a clinically demonstrated Dermal Regeneration Template.
INTEGRA® Dermal Regeneration Template (IDRT-TS) is a bilayer membrane system for skin replacement. It has been designed for the treatment of full thickness lesions in a two-step procedure.
The temporary epidermal substitute layer on top of the matrix is made up of a thin silicone layer to control moisture loss from the wound; after 14 to 28 days it can be removed and the newly formed neo-dermis is covered with a split thickness skin graft to achieve final epithelial closure.
Indications
Integra Template is indicated for the postexcisional treatment of full-thickness and partial-thickness injuries where sufficient autograft is not available at the time of excision or not desirable due to the physiological condition of the patient. Integra Template is also indicated for use in reconstruction of postexcisional, full-thickness defects of the integument where there is, in the opinion of the treating surgeon, a potential benefit to the patient by improving the reconstructive outcome or decreasing their mortality/morbidity.
Contraindications
The use of Integra Template is contraindicated in patients with known hypersensitivity to bovine collagen, chondroitin sulfate derived from shark cartilage, or silicone materials.
Integra Template should not be used on clinically diagnosed infected wounds.
Ordering Information
- Each sheet of INTEGRA template is packaged in phosphate buffer in a foil pouch.
- Each foil pouch is packaged in a sealed outer chevron-style pouch.
- Store flat at +2º to +30ºC.
- Protect from freezing.
- Once the product packaging has been opened, the product cannot be stored for reuse.
- Please refer to the clinical training materials for complete instructions.
| Catalog No. | Size | Quantity |
|---|---|---|
| 82021 | IDRT-SL 5cm x 5cm | 1 sheet |
| 84051 | IDRT-SL 10cm x 12,5cm | 1 sheet |
| 84101 | IDRT-SL 10cm x 25cm | 1 sheet |
| 88101 | IDRT-SL 20cm x 25cm | 1 sheet |
Product Catalogues
N/A
Regulatory Information
Class III
Integra LifeSciences Corporation
311 Enterprise Drive
Plainsboro • NJ 08536 • USA
Integra LifeSciences Services (France)
Immeuble Sequoia 2 • 97 allée Alexandre Borodine
Parc technologique de la Porte des Alpes
69800 Saint Priest • FRANCE
Phone: +33 (0)4 37 47 59 50 • fax: +33 (0)4 37 47 59 30
integralife.eu
CE 0086
Legal information
Availability of these products might vary from a given country or region to another, as a result of specific local regulatory approval or clearance requirements for sale in such country or region.
• Consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions and instructions for use.
• Non contractual document. Integra reserves the right, without prior notice, to modify the products in order to improve their quality.
• Warning: Applicable laws restrict these products to sale by or on the order of a physician.
Please contact Integra customer service should you need any additional information on devices classification. All the medical devices mentioned on this document are CE marked according to European council directive 93/42/ EEC on medical devices and its relatives, unless specifically identified as “NOT CE MARKED”.
Integra and the Integra logo are registered trademarks of Integra LifeSciences Corporation or its subsidiaries in the USA and/or other countries. ©2018 Integra LifeSciences Corporation. All rights reserved.
Last modification date: 02/2018. 0858813-1-EN
Document for use in Europe, Middle-East & Africa only.
For complete product information, please consult product labels and inserts for any indications, contraindications, hazards, warnings, precautions, and instructions for use.
