Uncoated medium weight monofilament polypropylene mesh on the anterior side with an absorbable hydrogel ® barrier based on Sepra Technology on the posterior side for laparoscopic ventral hernia repair.
Uncoated medium weight monofilament polypropylene mesh on the anterior side with an absorbable hydrogel barrier based on Sepra® Technology on the posterior side for laparoscopic ventral hernia repair.
Uncoated medium weight monofilament polypropylene mesh on the anterior side with an absorbable hydrogel ® barrier based on Sepra Technology on the posterior side for laparoscopic ventral hernia repair.
Efficient
Effective
Minimal contraction shown in preclinical testing compared to a leading microporous absorbable barrier mesh
At 4 weeks, Ventralight™ ST Mesh demonstrated 42% less area meshcontracture than a competitive macroporous absorbable barrier mesh.
Results were statistically significant.*
Proven
Ventralight™ Absorbable Barrier based on Sepra® Technology
Strong tissue Proven incorporation
The open-pore design of the uncoated monofilament polypropylene in Ventralight™ ST Mesh allows for:
* Preclinical data on file at BD. Results may not correlate to performance in humans.
** Based on a preclinical study of a composite polypropylene/ePTFE hernia repair mesh.
INDICATIONS
Ventralight™ ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.
CONTRAINDICATIONS
WARNINGS
>strong>ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation, infection, allergic reaction, and recurrence of the hernia or soft tissue defect.
Please consult package insert for more detailed safety information and instructions for use.
BD-14799
* Preclinical data on file at BD. Results may not correlate to performance in humans.
** Based on a preclinical study of a composite polypropylene/ePTFE hernia repair mesh.
INDICATIONS
Ventralight™ ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.
CONTRAINDICATIONS
WARNINGS
>strong>ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation, infection, allergic reaction, and recurrence of the hernia or soft tissue defect.
Please consult package insert for more detailed safety information and instructions for use.
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* Preclinical data on file at BD. Results may not correlate to performance in humans.
** Based on a preclinical study of a composite polypropylene/ePTFE hernia repair mesh.
INDICATIONS
Ventralight™ ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias.
CONTRAINDICATIONS
WARNINGS
>strong>ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation, infection, allergic reaction, and recurrence of the hernia or soft tissue defect.
Please consult package insert for more detailed safety information and instructions for use.