Intramesh® T1
Repair and parietal reinforcement of umbilical and ventral hernias. Intra-peritoneal implantation.
Intramesh® T1
Repair and parietal reinforcement of umbilical and ventral hernias. Intra-peritoneal implantation.
Descriptions
Technical specifications
Descriptions
These products can be used in laparoscopic surgery or open surgery. INTRAMESH® T1 products have a non-adhesive side, which is designed to avoid or reduce visceral adherences during intra peritoneal use or extra peritoneal use in the presence of a peritoneal defect. Marking in black ink, composed of a cross and dots is on the non-adhesive side. The meshes, biocompatible and non resorbable have the advantage of having a shape memory and a gread flexibility.
Technical specifications
Composition
One side made of monofilament polypropylene and one side made of expanded PTFE (ePTFE)
Surface mass
120 ± 23g/m²
Legal notice: Intramesh T1 is a class IIb medical devices manufactured by COUSIN BIOTECH s.a.s. The CE conformity has been carried out by the notified body SGS Belgium NV (CE1639). The management system of COUSIN BIOTECH S.A.S is certified for compliance with ISO 13485 standard. Please read carefully the instructions for use before using the device. Cousin Biotech is the legal manufacturer of the medical devices proposed by Cousin Surgery.
| Ref. | Size (cm) |
| FBIOT11515 | 15 x 15 |
| FBIOT12020 | 20 x 20 |
| FBIOT13030 | 30 x 30 |
| FBIOT13050 | 30 x 50 |
| FBIOT11015 | 10 x 15 |
| FBIOT11520 | 15 x 20 |
| FBIOT12025 | 20 x 25 |
| FBIOT1R12X | Ø 12 |
