We are MELEKIRMAK MEDICAL PRODUCTS CO. LTD based in istanbul ,Turkey. We are member of Tradekey.com since February, 2011. Ourbusiness is related to Beauty & Personal Care industry and wespecifically deal in medical consumables,medical products, medicaldevices,latex &nitrile gloves, polypropelene meshes,laparoscopic instruments, oncology products , urology products,.Please find our product details below: MELEKIRMAK CHEMYPROTECT18& MELEKIRMAK HIGH RISK NITRILE8 high risk nitrile examinationgloves, latex examnination gloves, chemotherapy gloves, for thepreparation of cytotoxic drugs, MELEKIRMAK POLYPROPELENE MONOLENEMESH DESCRIPTION: MELEKIRMAK MONOLENE MESH is constructed ofknitted filaments of extruded Polypropylene, a synthetic linearpoly-olefin (C3 H6) n identical in composition. MONOLENE MESH isavailable undyed in a variety ofsquare and rectangular sizes forsurgical procedures. The mesh is approximately 0.5mm ***** MONOLENEMESH is knitted by a process which interlinks each fiber junctionand provides for elasticity in both directions. This constructionpermits the mesh to be cut into any desired shape or size withoutunraveling. The fiber junctions are not subject to the same workfatigue exhibited by more rigid metallic meshes. This bidirectionalextendable property allows adaptation to various stressesencountered in the body. This material, when used has been reportedto be minimally reactive and to retain its strength for anindefinite period in clinical use. The mesh has high burst strengthof 12 kg/cm'.to 14 kg/cm2. PERFORMANCE: MELEKIRMAK MONOLENE MESHis a non absorbable mesh, used to span and reinforce traumatic orsurgicalwounds to provide extended support during and followingwound healing. This mesh elicits minimal inflammatory reaction,which is transient and is followed by the deposition of a thinfibrous layer of tissue which can grow through the interstices ofthe mesh, thus incorporating the mesh into the adjacent tissue. Themesh remains soft and pliable and the wound healing is notnoticeably impaired. The mesh is not absorbed nor is subject todegradation or weakening by the action of tissue enzymes.INDICATIONS: MELEKIRMAK MONOLENE MESH may be used for the repair ofhernia, uterovaginal prolapse, endoscopic procedures and otherfacial deficiencies that require the addition of a reinforcing orbridging material to obtain the desired surgical result.APPLICATION: It is recommended that non absorbable sutures orstaples be placed 6.5 to 12.5mm apart at a distance approximately6.5mm from the edge of the mesh. Some surgeons prefer to suture anuncut section of the mesh that is considered larger than the defectinto position over the wound. The opposite sides are then suturedto assure proper closure under correct tension. When the marginsutures have all been placed, the extra mesh is trimmed away.CONTRA INDICATIONS: When this mesh is used in infants or childrenwith future growth potential, the surgeon should be aware that thisproduct will not stretch significantly as the patient *****MONOLENE MESH in contaminated wounds should be used with theunderstanding that subsequent infection may require removal of thematerial. WARNING: Users should be familiar with surgicalprocedures and techniques involving non absorbable meshes beforeemploying MELEKIRMAK MONOLENE MESH for wound closure. Acceptablesurgical practice should be followed for the management of infectedor contaminated wounds. MELEKIRMAK MONOLENE MESH is supplied as asterile product. Resterilization is not recommended. However whenthe mesh is not used immediately after removal from the pack, itcan be subject to conventional method of sterilizing in anautoclave at 1210 centigrade for 20 minutes before use. lf thismesh is stained with blood or soiled, it should not be sterilizedfor reuse. PRECAUTIONS: Minimum of 6.5mm of mesh should extendbeyond the suture line. ADVERSE REACTIONS: Adverse reactions arethose associated with surgically implantable materials whichinclude infection potentiation, inflammation, adhesion formation,fistula formation and extrusion. MELEKIRMAK POLYPROPELENE MONOLENEMESH DESCRIPTION: MELEKIRMAK MONOLENE MESH is constructed ofknitted filaments of extruded Polypropylene, a synthetic linearpoly-olefin (C3 H6) n identical in composition. MONOLENE MESH isavailable undyed in a variety ofsquare and rectangular sizes forsurgical procedures. The mesh is approximately 0.5mm ***** MONOLENEMESH is knitted by a process which interlinks each fiber junctionand provides for elasticity in both directions. This constructionpermits the mesh to be cut into any desired shape or size withoutunraveling. The fiber junctions are not subject to the same workfatigue exhibited by more rigid metallic meshes. This bidirectionalextendable property allows adaptation to various stressesencountered in the body. This material, when used has been reportedto be minimally reactive and to retain its strength for anindefinite period in clinical use. The mesh has high burst strengthof 12 kg/cm'.to 14 kg/cm2. PERFORMANCE: MELEKIRMAK MONOLENE MESHis a non absorbable mesh, used to span and reinforce traumatic orsurgicalwounds to provide extended support during and followingwound healing. This mesh elicits minimal inflammatory reaction,which is transient and is followed by the deposition of a thinfibrous layer of tissue which can grow through the interstices ofthe mesh, thus incorporating the mesh into the adjacent tissue. Themesh remains soft and pliable and the wound healing is notnoticeably impaired. The mesh is not absorbed nor is subject todegradation or weakening by the action of tissue enzymes.INDICATIONS: MELEKIRMAK MONOLENE MESH may be used for the repair ofhernia, uterovaginal prolapse, endoscopic procedures and otherfacial deficiencies that require the addition of a reinforcing orbridging material to obtain the desired surgical result.APPLICATION: It is recommended that non absorbable sutures orstaples be placed 6.5 to 12.5mm apart at a distance approximately6.5mm from the edge of the mesh. Some surgeons prefer to suture anuncut section of the mesh that is considered larger than the defectinto position over the wound. The opposite sides are then suturedto assure proper closure under correct tension. When the marginsutures have all been placed, the extra mesh is trimmed away.CONTRA INDICATIONS: When this mesh is used in infants or childrenwith future growth potential, the surgeon should be aware that thisproduct will not stretch significantly as the patient *****MONOLENE MESH in contaminated wounds should be used with theunderstanding that subsequent infection may require removal of thematerial. WARNING: Users should be familiar with surgicalprocedures and techniques involving non absorbable meshes beforeemploying MELEKIRMAK MONOLENE MESH for wound closure. Acceptablesurgical practice should be followed for the management of infectedor contaminated wounds. MELEKIRMAK MONOLENE MESH is supplied as asterile product. Resterilization is not recommended. However whenthe mesh is not used immediately after removal from the pack, itcan be subject to conventional method of sterilizing in anautoclave at 1210 centigrade for 20 minutes before use. lf thismesh is stained with blood or soiled, it should not be sterilizedfor reuse. PRECAUTIONS: Minimum of 6.5mm of mesh should extendbeyond the suture line. ADVERSE REACTIONS: Adverse reactions arethose associated with surgically implantable materials whichinclude infection potentiation, inflammation, adhesion formation,fistula formation and extrusion. latex nitrile examination gloveshigh risk nitrile examination gloves, latex examnination gloves,chemotherapy gloves, for the preparation of cytotoxic drugs, Thankyou for taking the time to go through our business profile. Ifthere are any question, inquiry or comments, please feel free tocontact us.
