MatriDerm® by MedSkin Solutions Dr. Suwelack

Decision Tree

Is the wound clean?

Yes

Debridement
+ where appropriate systemic antibiotics

Is the patient high risk for general anesthesia due to comorbidities?

Yes **

Is the wound bed well vascularized?

Yes

Use NPWT and / or adjuncts to improve vascularity of wound bed

Is the wound highly exuding?

Yes

Is the cavity deeper than 5mm?

Yes

e.g. legs, trunk, upper arm

e.g. face, hands, feet, forearm, scalp

Large area of exposed bones/tendons

Yes

Large area of exposed bones/tendons

Yes

	Ref. No	Size
A4	83420-200	210 x 297 x 2mm
83430-200	210 x 297 x 3mm
A6	83421-200	105 x 149 x 2mm
83431-200	105 x 149 x 3mm
A8	83422-200	52 x 74 x 2mm
83432-200	52 x 74 x 3mm
A9	83423-200	37 x 52 x 2mm
83433-200	37 x 52 x 3mm

	Ref. No	Size
A4	83460-200	210 x 297 x 2mm
83470-200	210 x 297 x 3mm
A6	83461-200	105 x 149 x 2mm
83471-200	105 x 149 x 3mm
A8	83462-200	52 x 74 x 2mm
83472-200	52 x 74 x 3mm
A9	83463-200	37 x 52 x 2mm
83473-200	37 x 52 x 3mm

	Ref. No	Size
A4	83410-200	210 x 297 x 1mm
A6	83411-200	105 x 149 x 1mm
A8	83412-200	52 x 74 x 1mm
A9	83413-200	37 x 52 x 1mm

	Ref. No	Size
A4	83440-200	210 x 297 x 1mm
A6	83441-200	105 x 149 x 1mm
A8	83442-200	52 x 74 x 1mm
A9	83443-200	37 x 52 x 1mm

	Ref. No	Size
A4	83410-200	210 x 297 x 1mm
A6	83411-200	105 x 149 x 1mm
A8	83412-200	52 x 74 x 1mm
A9	83413-200	37 x 52 x 1mm

	Ref. No	Size
A4	83440-200	210 x 297 x 1mm
A6	83441-200	105 x 149 x 1mm
A8	83442-200	52 x 74 x 1mm
A9	83443-200	37 x 52 x 1mm

* This applies to both local and general anesthesia
** Irrespective of depth of cavity and degree of exposed bones / tendons
*** Depending on surgeon‘s experience and patient factors

All images courtesy of Prof. Dr. Adrian Dragu, Dresden, Germany

Clinical Application

Learn in this video how to reconstruct the Extensive and Widespread Paget’s Disease of the Breast (Cancer) with MatriDerm® in a Two-Step Procedure

Learn in this video the single steps of a One-Step Procedure from wound bed preparation till grafting the wound with STSG.

Learn in this video the single steps of a One-Step Procedure from wound bed preparation til grafting the wound with STSG.

Learn in this video the single steps of a One-Step Procedure from wound bed preparation till grafting the wound with STSG.

Bibliography

There are more than 170 publications on the efficacy of MatriDerm®. The bibliography gives an overview of the abstracts of the most important publications on MatriDerm®.

MatriDerm Bibliography

Mode of Action Watch video

In a One- or Multi-Step Procedure, MatriDerm ® Dermal Matrix is placed on the wound bed and covered with a secondary dressing of choice (e.g. split-thickness skin graft).

MatriDerm® Dermal Matrix provides a native three-dimensional collagen elastin matrix to facilitate cell migration and guided healing.

Fibroblasts are guided by the native collagen elastin scaffold ensuring structured healing and formation of a neo-dermis.

Enhanced neo-angiogenesis and formation of microvessels ensuring supply and optimal split-thickness skin graft take.

Manufacturer

MedSkin Solutions Dr. Suwelack AG www.medskin-suwelack.com Josef-Suwelack-Strasse 2 48727 Billerbeck Germany

Phone: +49 2543 21820
Fax: +49 2543 2182150
E-mail: info@medskin-suwelack.com
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Legal Information: Availability of all MatriDerm® 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. MedSkin Solutions Dr. Suwelack AG 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 MedSkin Solutions Dr. Suwelack AG customer service should you need any additional information on devices classiﬁcation. Products mentioned in this document are CE class III devices. 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”.