DynaMesh®

Tailored Implants Made of PVDF

DynaMesh®-ENDOLAP 3D

DynaMesh®-ENDOLAP 3D and DynaMesh®-ENDOLAP 3D visible implants are intended for the surgical treatment of inguinal or femoral hernias and permanently bridge and reinforce the soft tissue in the groin region in the area of the hernia defect.


DynaMesh®-ENDOLAP 3DProduct RangeUse and PropertiesVideosFurther Product Information

DM-endolap3d-optimised-shape-web

3D Shape
The device is a preformed three-dimensional mesh with a green central longitudinal marking, a green edge marking and centrally attached green filament ends.

Standardised Positioning
The device must be placed in such a way that the central green longitudinal marking is aligned with the inguinal ligament, the green central filament ends are located in projection to the junction of the inferior epigastric blood vessels to the external iliac blood vessels, and the green edge marking points dorsocaudally. The green filament ends must point to the user.

DM-endolap3d-curvator-web

Varying Pore Size
The pore size of the device varies laterally to the longitudinal marking.

When selecting and cutting the device, sufficient defect overlap must be ensured to minimise the likelihood of the hernia recurring.

DynaMesh®-ENDOLAP 3D 09 cm x 14 cm PV130914F1/F3
DynaMesh®-ENDOLAP 3D 10 cm x 15 cm regular PV131015F1/F3
DynaMesh®-ENDOLAP 3D 12 cm x 17 cm PV131217F1/F5
DynaMesh®-ENDOLAP 3D visible 09 cm x 14 cm PV120914F1/F3
DynaMesh®-ENDOLAP 3D visible 10 cm x 15 cm PV121015F1/F3
DynaMesh®-ENDOLAP 3D visible 12 cm x 17 cm PV121217F1
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Can be used both for the right and the left side.
Product DynaMesh®-ENDOLAP 3D (1)
DynaMesh®-ENDOLAP 3D visible (2)
Surgical Treatment Inguinal Hernias / Femoral Hernias
Surgical Approach Laparoscopic / Endoscopic
Surgical Technique TAPP / TEP
Mesh Position Preperitoneal (Posterior)
Fixation (None)* / Sutures / Tissue Adhesives / Tacks
Green Central and Edge Marking gruene_punkte
Visible Technology graue_punkte (1) / gruene_punkte (2)
Materials – Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (w/w) (1) (2)
– Phthalocyanine green (CAS 1328-53-6) < 1% (w/w) (1) (2)
– Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w) (2)
Polymer (Monofilament)
PVDF
Biocompatibility gruene_punkte [TR1]
Ageing Resistance
gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Tear Propagation Resistance gruene_punkte[TR21]
Effective Porosity
gruene_punkte High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR23]
Klinge’s Mesh Classification Class 1a [102P, TR23]
* Based on current knowledge, with the exception of large direct inguinal hernias (European
Hernia Society classification: M3), it appears possible to dispense with any form of fixation.
gruene_punkte Applies to all product sizes
gaue_punkte Does not apply
[#] Reference “#”(see “References”)
[TR#] Internal test report (see “internal test report references”)
Limitations “A” animal trial, “B” bench test, “VIT” in-vitro trial,
“P” published results based on the analysis of human mesh explants,
“PB” published results mainly based on bench tests

DynaMesh® Catalogue

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