DynaMesh®

Tailored Implants Made of PVDF

DynaMesh®-VASA

DynaMesh®-VASA is intended to be used as bridging material and/or ligament reinforcement of the uterosacral ligaments as part of surgical treatment for apical pelvic organ prolapse.


DynaMesh®-VASAProduct RangeUse and PropertiesVideosFurther Product Information

DynaMesh®-VASA

The device is used for bilateral sacropexy. In bilateral sacropexy, both of the uterosacral ligaments are reconstructed along their original course.


DynaMesh®-IVT01


DynaMesh®-IVT02

The following reusable instruments for retroperitoneal insertion are available separately for positioning:

DynaMesh®-IVT01 and DynaMesh®-IVT02

 

DynaMesh®-VASA
02 cm x 03 cm PV740203F1/F3
  FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Product DynaMesh®-VASA
Surgical Treatment Apical Pelvic Organ Prolapse (Uterus / Vaginal Stump / Cervical Stump)
Surgical Approach Minimally Invasive / Open
Surgical Technique Bilateral Sacropexy (reconstruction of both uterosacral ligaments)
Fixation – Anterior longitudinal ligament: non-absorbable suture or tacks
– Vaginal stump or cervix: non-absorbable suture
Smooth Warp-Knitted Selvedges
gruene_punkte
Defined Elasticity
gruene_punkte [TR100]
Visible Technology
gruene_punkte
Materials – Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (w/w)
– Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w)
Polymer (Monofilament) PVDF
Biocompatibility gruene_punkte [TR1]
Ageing Resistance gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Effective Porosity gruene_punkteHigh effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR101]
Klinge’s Mesh Classification Class 1a
[102P, TR101]
gruene_punkte Applicable
[#] 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

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-PRP

DynaMesh®-PRP soft and DynaMesh®-PRP visible implants are intended to be used as bridging material and reinforce soft tissue as part of surgical treatment for apical pelvic organ prolapse.


DynaMesh®-PRPProduct RangeUse and PropertiesVideosFurther Product Information

 

Pectopexy
Bilateral Fixation on the Pectineal Ligament

Fig. left:
Apical mesh repair following hysterectomy with DynaMesh®-PRP soft / visible (03 cm x 15 cm)


Pectopexy after vaginal/cervical stump prolapse:

  • Two implant sizes are available in the following dimensions DynaMesh®-PRP soft / visible 03 cm x 15 cm and DynaMesh®-PRP visible 03 cm x 18 cm.
  • With greatly shortened vaginas, e.g., following a radical hysterectomy, DynaMesh®-PRP visible 03 cm x 18 cm can be used.

Pectopexy after vaginal/cervical stump prolapse with concomitant cystocele and/or rectocele: (pulsion cystocele / rectocele)

  • Additional stabilisation of the anterior and/or posterior vaginal wall can be achieved with DynaMesh®-PRP visible 17 cm x 15 cm.

Pectopexy after uterine prolapse with uterine preservation:

  • With a normal sized uterus, DynaMesh®-PRP visible 03 cm x 18 cm can be used and fixed in place on the posterior cervix.

Pectopexy after uterine prolapse with uterine preservation:

  • With smaller uteri (below 100 g), anterior fixation of DynaMesh®-PRP soft / visible 03 cm x 15 cm can be selected as an alternative.
DynaMesh®-PRP soft (1) 03 cm x 15 cm PV540315F1/F3
DynaMesh®-PRP visible (2) 03 cm x 15 cm PV780315F1
DynaMesh®-PRP visible (3) 03 cm x 18 cm PV780318F1/F3
DynaMesh®-PRP visible) (4) 17 cm x 15 cm PV781715F1/F3
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Product DynaMesh®-PRP soft 03 cm x 15 cm (1)
DynaMesh®-PRP visible 03 cm x 15 cm (2)
DynaMesh®-PRP visible 03 cm x 18 cm (3)
DynaMesh®-PRP visible 17 cm x 15 cm (4)
Surgical Treatment Apical Pelvic Organ Prolapse (Uterus / Vaginal Stump / Cervical Stump)
Surgical Approach Minimally Invasive / Open
Surgical Technique Pectopexy (1) – (3) /
Pectopexy with reinforcement of the vaginal walls in case of concomitant cystocele and/or rectocele.(4)
Fixation – Pectineal ligament: non-absorbable suture
– Vaginal stump: absorbable monofilament suture
– Cervix: non-absorbable suture (size 0)
Smooth Warp-Knitted Selvedges gruene_punkte
Defined Elasticity gruene_punkte [TR120]
Visible Technology graue_punkte (1) / gruene_punkte (2) – (4)
Materials
– Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (w/w) (1) – (4)
– Phthalocyanine green (CAS 1328-53-6) < 1% (w/w) (1) – (4)
– Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w) (2) – (4)
Polymer (Monofilament) PVDF
Biocompatibility gruene_punkte [TR1]
Ageing Resistance gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Effective Porosity gruene_punkte High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR121]
Klinge’s Mesh Classification Class 1a [102P, TR121]
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

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-CESA

DynaMesh®-CESA is intended to be used as bridging material and/or ligament reinforcement of the uterosacral ligaments as part of surgical treatment for apical pelvic organ prolapse.


DynaMesh®-CESAProduct RangeUse and PropertiesVideosFurther Product Information

DynaMesh®-CESA

The device is used for bilateral sacropexy. In bilateral sacropexy, both of the uterosacral ligaments are reconstructed along their original course.


DynaMesh®-IVT01


DynaMesh®-IVT02

The following reusable instruments for retroperitoneal insertion are available separately for positioning:

DynaMesh®-IVT01 and DynaMesh®-IVT02

 

DynaMesh®-CESA
03 cm x 04 cm PV740404F1/F3
  FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Product DynaMesh®-CESA
Surgical Treatment Apical Pelvic Organ Prolapse (Uterus / Vaginal Stump / Cervical Stump)
Surgical Approach Minimally Invasive / Open
Surgical Technique Bilateral Sacropexy (reconstruction of both uterosacral ligaments)
Fixation – Anterior longitudinal ligament: non-absorbable suture or tacks
– Vaginal stump or cervix: non-absorbable suture
Smooth Warp-Knitted Selvedges
gruene_punkte
Defined Elasticity
gruene_punkte [TR100]
Visible Technology
gruene_punkte
Materials – Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (w/w)
– Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w)
Polymer (Monofilament) PVDF
Biocompatibility gruene_punkte [TR1]
Ageing Resistance gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Effective Porosity gruene_punkteHigh effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR101]
Klinge’s Mesh Classification Class 1a
[102P, TR101]
gruene_punkte Applicable
[#] 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

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-PRS

DynaMesh®-PRS soft and DynaMesh®-PRS visible implants are intended to be used as bridging material and reinforce the soft tissue of the vaginal walls as part of surgical treatment for apical pelvic organ prolapse.


DynaMesh®-PRSProduct RangeUse and PropertiesVideosFurther Product Information

Application Examples:

DM-PRS-sacrocolpopexy-uterus-vaginal-prolaps

Colpo-/cervicosacropexy

  • unilateral

Colpo-/cervicosacropexy

  • unilateral
  • anterior/posterior mesh plasty (for concomitant cystocele/rectocele)

Colpo-/cervicosacropexy

  • unilateral
DynaMesh®-PRS soft
02 cm x 16 cm PV350216F1
DynaMesh®-PRS soft 03 cm x 23 cm PV350323F1
DynaMesh®-PRS visible
03 cm x 23 cm PV750323F1/F10
DynaMesh®-PRS visible 3.3 cm x 24 cm PV750424F1/F10
DynaMesh®-PRS visible 04 cm x 20 cm PV750420F1/F10
DynaMesh®-PRS soft
05 cm x 27 cm PV350527F1
  FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Product DynaMesh®-PRS soft (1)
DynaMesh®-PRS visible (2)
Surgical Treatment Apical Pelvic Organ Prolapse (Vaginal Stump / Cervical Stump)
Surgical Approach Minimally Invasive / Open
Surgical Technique Sacropexy
Fixation – Anterior longitudinal ligament: non-absorbable suture or tacks
– Vaginal/cervical stump and vaginal walls: interrupted non-absorbable suture
Smooth Warp-Knitted Selvedges gruene_punkte
Defined Elasticity
gruene_punkte [TR130]
Visible Technology graue_punkte (1) / gruene_punkte (2)
Materials
– Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 99% (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]
Effective Porosity gruene_punkte High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR132]
Klinge’s Mesh Classification Class 1a [102P, TR132]
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

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-IPST

DynaMesh®-IPST, DynaMesh®-IPST visible, DynaMesh®-IPST-D visible, DynaMesh®-IPST-R and DynaMesh®-IPST-R visible implants are intended for the surgical treatment of parastomal hernias, and the prevention (not DynaMesh®-IPST-R or DynaMesh®-IPST-R visible) of parastomal hernias following ostomy surgery, and permanently bridge and reinforce the soft tissue of the abdominal wall in the area of the stoma.


DynaMesh®-IPSTProduct RangeUse and PropertiesVideosFurther Product Information

ipst-intraperitoneal

 

 

3D Funnel
The device has a passage point with a connected funnel for the passage of the intestine. The base area of the device must be positioned in contact with the tissue, as flat and smooth as possible, with the funnel pointing in the direction of the abdominal cavity.
When selecting the device, the diameter of the passage point should be chosen so that the intestine is tightly sheathed in the funnel.

 

 

 

 

Prefabricated Slit & Smooth Warp-Knitted Selvedges
Only DynaMesh®-IPST-R and DynaMesh®-IPST-R visible have a one-sided slit along the funnel and the base area (mesh flaps), starting from the passage point.
During positioning, the tight sheathing of the intestine in the funnel is achieved through appropriate overlapping of the mesh flaps with non-absorbable closure of the aperture.

 

 

Prevention and Repair of Parastomal Hernia

The diameter of the mesh funnel should be chosen so that the intestine is tightly sheathed. In repair, sufficient defect overlap and coverage of the base of the passage is necessary. When using DynaMesh®-IPST-D visible, attention must be paid to the side specificity (left-sided/right-sided stoma).

DynaMesh®-IPST Funnel length: 4.0 cm ø 02 cm x 15 cm x 15 cm (L4) IP072415F1
DynaMesh®-IPST Funnel length: 2.5 cm ø 02 cm x 15 cm x 15 cm IP070215F1
DynaMesh®-IPST Funnel length: 2.5 cm ø 02 cm x 25 cm x 25 cm IP070225F1
DynaMesh®-IPST Funnel length: 2.5 cm ø 03 cm x 16 cm x 16 cm IP070316F1
DynaMesh®-IPST Funnel length: 2.5 cm ø 04 cm x 17 cm x 17 cm IP070417F1
DynaMesh®-IPST visible Funnel length: 4.0 cm ø 02 cm x 15 cm x 15 cm (L4) IP082415F1
DynaMesh®-IPST visible Funnel length: 2.5 cm ø 02 cm x 15 cm x 15 cm IP080215F1
DynaMesh®-IPST visible Funnel length: 2.5 cm ø 03 cm x 16 cm x 16 cm IP080316F1
DynaMesh®-IPST-D visible Funnel length: 4.0 cm ø 02 cm x 30 cm x 30 cm (L4) left

Important: Side specificity (left-sided/right-sided stoma)

IP082431F1
DynaMesh®-IPST-D visible Funnel length: 4.0 cm ø 02 cm x 30 cm x 30 cm (L4) right

Important: Side specificity (left-sided/right-sided stoma)

IP082432F1
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)

 


Repair of Parastomal Hernia

With DynaMesh®-IPST-R and DynaMesh®-IPST-R visible, a tight sheathing of the intestine is achieved by a suitable overlap of the mesh flaps with non-absorbable closure.

DynaMesh®-IPST-R Funnel length: 3.5 cm ø 03 cm x 16 cm x 16 cm (L3.5) IP103316F1
DynaMesh®-IPST-R visible Funnel length: 3.5 cm ø 03 cm x 16 cm x 16 cm (L3.5) IP113316F1
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
Product DynaMesh®-IPST (1)
DynaMesh®-IPST visible (2)
DynaMesh®-IPST-D visible (3)
DynaMesh®-IPST-R (4)
DynaMesh®-IPST-R visible (5)
Surgical Treatment Parastomal Hernia
(Repair / Prevention) (1) – (3) / (Repair) (4) (5)
Surgical Approach Minimally Invasive / Open
Surgical Technique Chimney Technique
Mesh Position Intraperitoneal
Fixation Suture / Tacks / No Fibrin Glue
Green Filament Ends
gruene_punkte
Smooth Warp-Knitted Selvedges graue_punkte (1) – (3) / gruene_punkte (4) (5)
Visible Technology
graue_punkte (1) (4) / gruene_punkte (2) (3) (5)
Materials – Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 85% (w/w) (1) – (5)
– Polypropylene (PP) (CAS 9003-07-0) < 13% (w/w) (1) – (5)
– Phthalocyanine green (CAS 1328-53-6) < 1% (w/w) (1) – (5)
– Triiron tetraoxide (CAS 1317-61-9) < 1% (w/w) (2) (3) (5)
Polymers (Monofilament) PVDF, PP
Biocompatibility
gruene_punkte [TR1]
Ageing Resistance
gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Effective Porosity
gruene_punkte High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR71]
Klinge’s Mesh Classification Class 1a [102P, TR71B]
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®-IPST implants (1)-(5) must be inserted via an appropriate minimally invasive or open approach and must be placed intraperitoneally.

DynaMesh®-IPST implants (1)-(5) have a parietal side and a visceral side. The parietal side is identified by green filament ends and consists of PVDF on the surface and a small proportion of PP, whereas the visceral side consists of PVDF on the surface.

When using DynaMesh®-IPST-D visible (3), attention must be paid to the side specificity (left-sided/right-sided stoma), through which a particularly large overlap in a cranial as well as in a medial direction is ensured.

When positioning DynaMesh®-IPST-R and DynaMesh®-IPST-R visible (4) (5), the tight sheathing of the intestine in the funnel is achieved through appropriate overlapping of the mesh flaps with non-absorbable closure of the aperture.

DynaMesh® Catalogue

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-IPOM

DynaMesh®-IPOM and DynaMesh®-IPOM visible implants are intended for the surgical treatment of epigastric hernias, umbilical or incisional hernias, and the treatment of parastomal hernias following ostomy surgery, and permanently bridge and reinforce the soft tissue of the abdominal wall in the area of the abdominal wall defect.


DynaMesh®-IPOMProduct RangeUse and PropertiesVideosFurther Product Information

DynaMesh®-IPOM and DynaMesh®-IPOM visible implants are primarily made of polyvinylidene fluoride (PVDF).
The mesh implants are warp-knitted using coloured and uncoloured polyvinylidene fluoride (PVDF) monofilaments and uncoloured polypropylene (PP) monofilaments.

 

Positioning
DynaMesh®-IPOM and DynaMesh®-IPOM visible implants have a parietal side and a visceral side. The parietal side is identified by the green filament ends and consists of PVDF on the surface and a small proportion of PP, whereas the visceral side consists of PVDF on the surface.

The mesh implant must be placed in such a way that the green filament ends are always oriented towards the abdominal wall. At the same time, the mesh implant must be oriented so that the green filament ends are cranial or caudal.

 

DM-IPOM_intraoperativei

Intraoperative view

 

Cutting/overlapping
When cutting, care must be taken to ensure that the parietal side of the device can still be identified without any doubt. With epigastric hernias, umbilical and parastomal hernias following ostomy surgery, it is crucial to overlap the hernia orifice, whereas with incisional hernias it is crucial to overlap the scar tissue.
For further information on cutting/overlapping, please refer to the instructions for use.

DynaMesh®-IPOM d 12 cm round IP070012F1/F3
DynaMesh®-IPOM 07 cm x 06 cm IP070706F1/F5
DynaMesh®-IPOM 10 cm x 15 cm IP071015F1/F3
DynaMesh®-IPOM 15 cm x 15 cm IP071515F1/F3/F5
DynaMesh®-IPOM 15 cm x 20 cm IP071520F1/F3/F5
DynaMesh®-IPOM 15 cm x 40 cm IP071540F1
DynaMesh®-IPOM 20 cm x 20 cm IP072020F1
DynaMesh®-IPOM 20 cm x 25 cm IP072025F1
DynaMesh®-IPOM 20 cm x 30 cm IP072030F1/F3
DynaMesh®-IPOM 28 cm x 37 cm IP072837F1
DynaMesh®-IPOM 30 cm x 30 cm IP073030F1
DynaMesh®-IPOM 30 cm x 45 cm IP073045F1
DynaMesh®-IPOM visible d 12 cm round IP080012F1/F3
DynaMesh®-IPOM visible 07 cm x 06 cm IP080706F5
DynaMesh®-IPOM visible 10 cm x 15 cm IP081015F1
DynaMesh®-IPOM visible 15 cm x 15 cm IP081515F1/F3
DynaMesh®-IPOM visible 15 cm x 20 cm IP081520F1/F3
DynaMesh®-IPOM visible 20 cm x 20 cm IP082020F1
DynaMesh®-IPOM visible 20 cm x 25 cm IP082025F1
DynaMesh®-IPOM visible 20 cm x 30 cm IP082030F1/F3
DynaMesh®-IPOM visible 28 cm x 37 cm IP082837F1
DynaMesh®-IPOM visible 30 cm x 30 cm IP083030F1
DynaMesh®-IPOM visible 30 cm x 45 cm IP083045F1
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
size: laterolateral x craniocaudal

Product DynaMesh®-IPOM (1)
DynaMesh®-IPOM visible (2)
Surgical Treatment Umbilical Hernias / Epigastric Hernias /
Incisional Hernias / Parastomal Hernias
Surgical Approach Minimally Invasive / Open
Mesh Position Intraperitoneal* according to the intraperitoneal onlay mesh technique (IPOM).
Fixation Suture / Tacks / No Fibrin Glue
Green Filament Ends gruene_punkte
Visible Technology graue_punkte (1) / gruene_punkte (2)
Materials – Polyvinylidene fluoride (PVDF) (CAS 24937-79-9) > 85% (w/w) (1) (2)
– Polypropylene (PP) (CAS 9003-07-0) < 13% (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)
Polymers (Monofilament) PVDF, PP
Biocompatibility
gruene_punkte [TR1]
Ageing Resistance
gruene_punkte [2A, 5VIT, 27A, 52VIT, 93A, 101]
Tear Propagation Resistance
gruene_punkte [TR62]
Effective Porosity
gruene_punkte High effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR64]
Klinge’s Mesh Classification Class 1a [102P, TR64]
* In particular cases with an extraperitoneal mesh position in which there is a risk of contact between the mesh implant and the intestine, the device may also be placed extraperitoneally in onlay, sublay and/or preperitoneal mesh position.
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®-IPOM and DynaMesh®-IPOM visible implants have a parietal side and a visceral side. The parietal side is identified by green filament ends and consists of PVDF on the surface and a small proportion of PP, whereas the visceral side consists of PVDF on the surface.

DynaMesh® Catalogue

Download as PDF (english)

Als pdf herunterladen (deutsch)

DynaMesh®-CICAT

DynaMesh®-CICAT and DynaMesh®-CICAT visible implants are intended for the surgical treatment of epigastric hernias, umbilical or incisional hernias, and the prevention of incisional hernias, and permanently bridge and reinforce the soft tissue of the abdominal wall in the area of the abdominal wall defect.


DynaMesh®-CICATProduct RangeUse and PropertiesVideosFurther Product Information

Anti-Slip Surface
The devices have an anti-slip surface that ensures stable positioning of the mesh with reduced fixation compared to other devices available on the market. [132PB, 133PB, 134]

Dynamometric Positioning
For the correct dynamometric positioning of the device, ensure that the green or black marking strips are in a cranio-caudal orientation.

High Effective Porosity
The devices have a high effective porosity, which is known to reduce inflammation and the risk of excessive scar formation. [103P, TR33, TR35]

 

The device must not be placed partially or completely intraperitoneally.

 

 

[#] 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

When selecting and cutting the device, sufficient defect/scar overlap must be ensured to minimise the likelihood of the hernia recurring. With epigastric hernias and umbilical hernias, it is crucial to overlap the hernia orifice, whereas with incisional hernias it is crucial to overlap the scar tissue.

DynaMesh®-CICAT d 10 cm round PV090010F1/F3
DynaMesh®-CICAT 05 cm x 06 cm PV090506F1/F5
DynaMesh®-CICAT 10 cm x 10 cm PV091010F1/F3/F5
DynaMesh®-CICAT 10 cm x 15 cm PV091015F5
DynaMesh®-CICAT 10 cm x 35 cm PV091035F1/F2
DynaMesh®-CICAT 15 cm x 15 cm PV091515F1/F3
DynaMesh®-CICAT 15 cm x 25 cm PV091525F1/F2/F5
DynaMesh®-CICAT 15 cm x 30 cm PV091530F1/F2/F5
DynaMesh®-CICAT 15 cm x 60 cm PV091560F1
DynaMesh®-CICAT 18 cm x 40 cm PV091840F2
DynaMesh®-CICAT 20 cm x 30 cm PV092030F1/F2/F5
DynaMesh®-CICAT 27 cm x 15 cm PV092715F1/F2
DynaMesh®-CICAT 30 cm x 30 cm PV093030F1/F2
DynaMesh®-CICAT 30 cm x 45 cm PV093045F1/F3
DynaMesh®-CICAT
40 cm x 20 cm PV094020F1/F2
DynaMesh®-CICAT 45 cm x 60 cm PV094560F1
DynaMesh®-CICAT visible d 10 cm round PV160010F3
DynaMesh®-CICAT visible 05 cm x 06 cm PV160506F1/F5
DynaMesh®-CICAT visible 07 cm x 35 cm PV160735F1/F5
DynaMesh®-CICAT visible 10 cm x 10 cm PV161010F3
DynaMesh®-CICAT visible 10 cm x 35 cm PV161035F2
DynaMesh®-CICAT visible 15 cm x 15 cm PV161515F3
DynaMesh®-CICAT visible 15 cm x 25 cm PV161525F2/F5
DynaMesh®-CICAT visible 15 cm x 30 cm PV161530F2
DynaMesh®-CICAT visible 18 cm x 40 cm PV161840F2
DynaMesh®-CICAT visible 20 cm x 30 cm PV162030F1/F2/F5
DynaMesh®-CICAT visible 30 cm x 45 cm PV163045F1/F3
DynaMesh®-CICAT visible 40 cm x 20 cm PV164020F1
DynaMesh®-CICAT visible 45 cm x 60 cm PV164560F1
FX = X unit(s)/box (e.g. F3 = 3 unit(s)/box)
size: laterolateral x craniocaudal
Product DynaMesh®-CICAT (1)
DynaMesh®-CICAT visible (2)
Surgical Treatment Epigastric Hernias / Umbilical Hernias / Incisional Hernias
Prevention: Incisional Hernia
Surgical Approach Minimally Invasive / Open
Mesh Position Extraperitoneal
(onlay, sublay and/or preperitoneal)
Fixation Sutures / Tacks / Tissue Adhesives
Marking Strips Green (1) / Black (2)
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)
– 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]
Dynamometric Properties
gruene_punkte [TR38, 128P, 129]
Tear Propagation Resistance
gruene_punkte [TR31]
Anti-Slip Surface
gruene_punkte [132PB, 133PB, 134]
Effective Porosity gruene_punkteHigh effective porosity reduces inflammation and the risk of excessive scar formation. [103P, TR33, TR35]
Klinge’s Mesh Classification Class 1a [102P, TR33, TR35]
DynaMesh®-CICAT implants must be placed extraperitoneally in onlay, sublay and/or preperitoneal mesh position.
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

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DynaMesh® Catalogue

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