Product Description : Amogel is a amorphous hydrogel dressing and is formulated with the vital ingredient carboxy methyl cellulose, Amogel gently hydrates dry necrotic tissues and facilitates autolyticdebridement. Amogel provides optimum moist environment to the wound bed and accelerates faster wound healing.

Salient Features :

• F Donates moisture to the wound bed
• F Absorbs wound exudate
• F Available in convenient lami tubes for precise, directable and controlled application
• F Possessing both absorption (moderate) and donation characteristics

Benefit :

• F Provides optimum moist wound environment for healing
• F Encourage and facilitates autolytic debridement
• F Desloughing action (assist in removal of devitalised tissue)
• F Minimisespain to patient during dressing change

Indications :

• F Minor burns
• F Supercial lacerations
• F Dry and Necrotic Wounds
• F Cuts and abrasions
• F Venous ulcers
• F Surgical incisions
• F Diabetic foot ulcers
• F Pressure sores

Contra-indications : Contra-indicated on heavily exuding wounds.

Application Methodology :

• F Prepare wound site as per the standard protocol
• F Irrigate wound with sterile saline solution to clean wound site
• F Bleeding should be controlled before application of Amogel

Application :

• Apply Amogel directly on to the wound bed, maintain aseptic conditions.
• Apply Amogel on to the wound bed evenly to a depth of approximately 5mm.
• Use appropriate secondary dressing as per choice and change the dressing based on the wound condition.

Introduction : Gelatin is a substantially pure protein food ingredient, obtained by the thermal degeneration of collagen, which are the structural mainstay and most common protein in the animal kingdom. Gelatin sponges have been used in clinical practice as hemostats for more than 50 years and been proven to be effective and safe as other types of haemostats. Due to the threat of BSE/TSE issues on Bovine origin materials, Porcine Gelatin Materials have been developed and now they are widely being used in Pharmaceutical Industry.

Product Description :

• Scrofalon® is a surgical haemostatic sponge, manufactured from highly purified neutral gelatin material exclusively from porcine origin for use in various surgical procedures, where traditional heamostasis is difficult or impractical and use of other non-absorbable materials are undesirable. Available in different convenient dimensions in Gamma sterilized form with suitable double sterile blister packaging or pouches for special sizes.
• Scrofalon® absorbs approximately 40-50 times, it's weight of water and adheres easily to the bleeding site. The uniform porosity
• Scrofalon® guarantees a favourable haemostasis. When implanted in vivo, it is completely absorbed within 3-4 weeks.
• Scrofalon® is non-toxic, non-allergenic, non-immunogenic, non-pyrogenic and meets the bicompatibility requirements as per EN ISO 10993 standards.

Indications :

• Plastic Surgery
• Neurosurgery
• General Surgery
• Dermatology
• ENT and Dental Surgery
• Gynaecology
• Orthopedics and Trauma
• Anorectal surgery
• Abdominal Surgery

Application & User Guide : Scrofalon® is white, pliable, light, and insoluble in water. It is removed from the package under strict aseptic conditions and can be cut to desired size, applied dry or saturated with physiologic. salt solution or thrombin or an antibiotic solution of the desired concentration. Squeeze the material between two fingers to remove the air bubbles so that the sponge, while immersed in the solution will regain its original size and shape almost immediately. At the time of use, the superfluous solution may be allowed to drip upon a gauze compress. The saturated sponge is then applied to the haemorrhage area and is then held in place with moderate pressure for 10-15 seconds. Usually the first application of Scrofalon® will control bleeding, but if not, additional applications should be made using fresh pieces of sponge. When bleeding is controlled, the pieces of Scrofalon® should be left in place, otherwise bleeding may start again. Since Scrofalon® causes little more cellular infiltration than the blood clot, the wound may be closed over it.

Contraindications : Scrofalon® should not be used in closure of skin incisions because it may interfere with the healing of skin edges.

Precautions & Warnings :

• Scrofalon® is a sterile product and should not be resterilised, as it would change the characteristics of the product.
• Discard the unused portions of the sponge.
• Use of Scrofalon. is not recommended for infected sites.
• By absorbing the fluid, the sponge may expand and thus impinge on neighboring structures. Hence, minimal pre-compression is advised when packing into cavities.
• In neuro surgery, it should not be left in closed cavities, since it may cause compression of the nervous tissues when it expands.
• While using Scrofalon® other normal homeostatic procedures including suture, pressure and ligature should be neglected.

Introduction : Surgeons who treat chronic non-healing ulcers including diabetic ulcers and pressure ulcers etc., face a real challenge when it comes to the closure of the wounds due to inadequacies of conventional treatment protocols and complexicities of ulcers. The result is catastrophic and traumatic. Quality of life suffers as many patients get into the stage of amputations especially in the case of diabetic foot ulcers. It is for this reason, useful biomaterials like collagen play a very important role in the wound management to alleviate the sufferings of millions of victims in the category.

Collagen : Collagen is an extra cellular matrix protein playing a major role in connective tissue. It is the most abundant protein in humans and performs multiple functions. In fish, the largest concentration of collagen is found in the skeleton, fins, skin and air bladder. Collagen as a biomaterial and its role in wound management is a well-documented subject. Collagen encourages wound healing through the deposition and organization of freshly formed fibers and granulation tissues in the wound bed and thus creating a very conducive environment for wound healing.

Role of Collagen in wound healing :

• F Stops Bleeding (Hovig et al., 1968)
• F Helps in wound debridement by attracting monocytes (Postlewaithe and Kang, 1976)
• F Provides a Matrix for Tissue and Vascular Growth (Kleinman et al, 1981a)
• F Attracts fibroblasts and helps in directed migration of cells (Dunn and Ebendal, 1978)
• F Binds with Fibronectin, which promotes cell binding (Kleinman et al., 1981b)
• F Supports growth (Morykwas et al., 1989), differentiation and migration (Emerman and Pitelka, 1977) of Keratinocytes
• F Helps in deposition of oriented and organized fibres (Doillion et al, 1981), which increase the integrity of the Tissue

Salient Features :

• F Highly absorbent
• F Derived from fish source - no threat of BSE/TSE
• F Biocompatible as per EN ISO 10993 Standards
• F Non-toxic, non-allergenic, non-immunogenic, non-pyrogenic
• F Collagen reduces wound pH
• F Resorbable haemostat
• F Facilitates the normal healing process
• F Absorbs exudate, reduces inflammation and oedema and allows
• gaseous exchange
• F As a natural stimulant for autolytic debridement
• F Transforms wounds from inflammation phase to remodeling phase
• F As a scaffold for tissue regeneration

Indications :

• F Pressure ulcers
• F Venous stasis ulcers
• F Diabetic ulcers
• F Acute wounds for example trauma and surgical wounds
• F Partial thickness burns
• F Moderate to heavily exuding wounds

Contraindications :

• F Do not apply Kolspon® on infected wounds
• F In case of infection, control with systemic antibiotics and resume the application
• F In case of irritation, remove and discontinue Kolspon®
• F Do not apply on patients hypersensitive to collagen

Application Methodology :

• F Ensure wound bed is thoroughly cleansed
• F Select the required dimension of Kolspon® depending upon the size and depth wound
• F Kolspon® can be applied dry or moist depending upon the type of wound bed
• F Secure the sponge with a secondary dressing of choice
• F For early removal or change of Kolspon®, irrigate with normal saline

Do not pack the wound tightly sponge is highly absorbent and need room for expansion. Always maintain a moist wound environment.

Product Description : Hydrez®-Plus is a silver impregnated hydrophilic foam dressing with a transparent breathable Polyurethane skin and soft silicone wound contact layer. The silicone wound contact layer is highly perforated thereby enabling the routine vertical absorption of exudates by the foam and also protecting the fragile wound bed from being macerated. Hydrez®-Plus is offered with & without an adhesive border.

Salient Features :

• F Painless removal or re-positioning
• F High Fluid handling capacity
• F Adhesive border dressing prevents the need of secondary dressing or fixators
• F High Patient compliance
• F Can be kept in place up to 4 days

 

Indications :

• F Moderate to Highly exuding wounds
• F Diabetic Ulcers
• F Pressure sores & ulcers
• F Traumatic wounds
• F Incision sites
• F Venous stasis ulcers
• F Post-operative Surgical sites
• F Lacerations & abrasions

Contraindications :

• F Hydrez®-Plus is not be surgically implanted.
• F Do not use Hydrez®-Plus on patients with a known sensitivity to silver, polyurethane foams of silicone.

Application Methodology :

• Prepare the wound bed as per your standard protocol. An initial debarment of the wound may be essential to ensure
• that the wound edges contain viable tissue.
• Always maintain moist wound environment. Ensure that wound bed is thoroughly cleansed and is free of debris and
• necrotic tissue.
• Sterile technique should always be used to remove Hydrez®-Plus from its packaging.
• Remove the release film and make sure HydrezTM-Plus overlaps the wound bed by at-least 2cm onto the surrounding
• skin. Apply the silicone adherent side on the wound.
• If use of Hydrez®-Plus with an adhesive dressing, there is no need of a secondary dressing or else Hydrez®-Plus
• can be secured with suitable secondary dressing or fixator.
• Hydrez®-Plus can be applied up to 4 days or changed according to the wound condition or the clinician's discretion.

Precautions and Warnings :

•  Product for use by Registered Medical Practitioner or a Hospital.
• Hydrez®-Plus is supplied as a sterile product and is strictly for single use only. Do not re-sterilize as the process may
• result in change of product characteristics.
• Unused, opened packages of Hydrez®-Plus should be discarded to avoid cross contamination and hospital acquired
• infection on the device upon storage.
• Sterility of Hydrez®-Plus is not guaranteed when the unused portion of the device is left in the pack.
• Ensure the dressing is applied to the wound pink side up.
• Securing of Hydrez®-Plus with occlusive films or tapes is not recommended, as these reduce moisture vapor loss,
• which may impair the effectiveness of the dressing.

Be it online payment processing or offline payment processing, we are capable of executing both as per your convenience. We take care of all your transactions made; by this, we make all the procedures transparent. Designed and developed using the premium raw material and modern work methods; we guarantee high quality standards and longevity of our products. Also, we make sure that the raw material is sourced from the trusted places.

We offer Neuskin sterile collagen membrane in dry form the bovine collagen membrane is offered in freeze dried form to avoid pre-treatment of collagen membrane in normal saline before application. It is gamma sterilized and available in different dimensions. Neuskin - trade mark under registration in india.

Product Description : Amogel is a amorphous hydrogel dressing and is formulated with the vital ingredient carboxy methyl cellulose, Amogel gently hydrates dry necrotic tissues and facilitates autolyticdebridement. Amogel provides optimum moist environment to the wound bed and accelerates faster wound healing.

Salient Features :

• F Donates moisture to the wound bed
• F Absorbs wound exudate
• F Available in convenient lami tubes for precise, directable and controlled application
• F Possessing both absorption (moderate) and donation characteristics

Benefit :

• F Provides optimum moist wound environment for healing
• F Encourage and facilitates autolytic debridement
• F Desloughing action (assist in removal of devitalised tissue)
• F Minimisespain to patient during dressing change

Indications :

• F Minor burns
• F Supercial lacerations
• F Dry and Necrotic Wounds
• F Cuts and abrasions
• F Venous ulcers
• F Surgical incisions
• F Diabetic foot ulcers
• F Pressure sores

Contra-indications : Contra-indicated on heavily exuding wounds.

Application Methodology :

• F Prepare wound site as per the standard protocol
• F Irrigate wound with sterile saline solution to clean wound site
• F Bleeding should be controlled before application of Amogel

Application :

• Apply Amogel directly on to the wound bed, maintain aseptic conditions.
• Apply Amogel on to the wound bed evenly to a depth of approximately 5mm.
• Use appropriate secondary dressing as per choice and change the dressing based on the wound condition.

Introduction : Gelatin is a substantially pure protein food ingredient, obtained by the thermal degeneration of collagen, which are the structural mainstay and most common protein in the animal kingdom. Gelatin sponges have been used in clinical practice as hemostats for more than 50 years and been proven to be effective and safe as other types of haemostats. Due to the threat of BSE/TSE issues on Bovine origin materials, Porcine Gelatin Materials have been developed and now they are widely being used in Pharmaceutical Industry.

Product Description :

• Scrofalon® is a surgical haemostatic sponge, manufactured from highly purified neutral gelatin material exclusively from porcine origin for use in various surgical procedures, where traditional heamostasis is difficult or impractical and use of other non-absorbable materials are undesirable. Available in different convenient dimensions in Gamma sterilized form with suitable double sterile blister packaging or pouches for special sizes.
• Scrofalon® absorbs approximately 40-50 times, it's weight of water and adheres easily to the bleeding site. The uniform porosity
• Scrofalon® guarantees a favourable haemostasis. When implanted in vivo, it is completely absorbed within 3-4 weeks.
• Scrofalon® is non-toxic, non-allergenic, non-immunogenic, non-pyrogenic and meets the bicompatibility requirements as per EN ISO 10993 standards.

Indications :

• Plastic Surgery
• Neurosurgery
• General Surgery
• Dermatology
• ENT and Dental Surgery
• Gynaecology
• Orthopedics and Trauma
• Anorectal surgery
• Abdominal Surgery

Application & User Guide : Scrofalon® is white, pliable, light, and insoluble in water. It is removed from the package under strict aseptic conditions and can be cut to desired size, applied dry or saturated with physiologic. salt solution or thrombin or an antibiotic solution of the desired concentration. Squeeze the material between two fingers to remove the air bubbles so that the sponge, while immersed in the solution will regain its original size and shape almost immediately. At the time of use, the superfluous solution may be allowed to drip upon a gauze compress. The saturated sponge is then applied to the haemorrhage area and is then held in place with moderate pressure for 10-15 seconds. Usually the first application of Scrofalon® will control bleeding, but if not, additional applications should be made using fresh pieces of sponge. When bleeding is controlled, the pieces of Scrofalon® should be left in place, otherwise bleeding may start again. Since Scrofalon® causes little more cellular infiltration than the blood clot, the wound may be closed over it.

Contraindications : Scrofalon® should not be used in closure of skin incisions because it may interfere with the healing of skin edges.

Precautions & Warnings :

• Scrofalon® is a sterile product and should not be resterilised, as it would change the characteristics of the product.
• Discard the unused portions of the sponge.
• Use of Scrofalon. is not recommended for infected sites.
• By absorbing the fluid, the sponge may expand and thus impinge on neighboring structures. Hence, minimal pre-compression is advised when packing into cavities.
• In neuro surgery, it should not be left in closed cavities, since it may cause compression of the nervous tissues when it expands.
• While using Scrofalon® other normal homeostatic procedures including suture, pressure and ligature should be neglected.

Introduction : Surgeons who treat chronic non-healing ulcers including diabetic ulcers and pressure ulcers etc., face a real challenge when it comes to the closure of the wounds due to inadequacies of conventional treatment protocols and complexicities of ulcers. The result is catastrophic and traumatic. Quality of life suffers as many patients get into the stage of amputations especially in the case of diabetic foot ulcers. It is for this reason, useful biomaterials like collagen play a very important role in the wound management to alleviate the sufferings of millions of victims in the category.

Collagen : Collagen is an extra cellular matrix protein playing a major role in connective tissue. It is the most abundant protein in humans and performs multiple functions. In fish, the largest concentration of collagen is found in the skeleton, fins, skin and air bladder. Collagen as a biomaterial and its role in wound management is a well-documented subject. Collagen encourages wound healing through the deposition and organization of freshly formed fibers and granulation tissues in the wound bed and thus creating a very conducive environment for wound healing.

Role of Collagen in wound healing :

• F Stops Bleeding (Hovig et al., 1968)
• F Helps in wound debridement by attracting monocytes (Postlewaithe and Kang, 1976)
• F Provides a Matrix for Tissue and Vascular Growth (Kleinman et al, 1981a)
• F Attracts fibroblasts and helps in directed migration of cells (Dunn and Ebendal, 1978)
• F Binds with Fibronectin, which promotes cell binding (Kleinman et al., 1981b)
• F Supports growth (Morykwas et al., 1989), differentiation and migration (Emerman and Pitelka, 1977) of Keratinocytes
• F Helps in deposition of oriented and organized fibres (Doillion et al, 1981), which increase the integrity of the Tissue

Salient Features :

• F Highly absorbent
• F Derived from fish source - no threat of BSE/TSE
• F Biocompatible as per EN ISO 10993 Standards
• F Non-toxic, non-allergenic, non-immunogenic, non-pyrogenic
• F Collagen reduces wound pH
• F Resorbable haemostat
• F Facilitates the normal healing process
• F Absorbs exudate, reduces inflammation and oedema and allows
• gaseous exchange
• F As a natural stimulant for autolytic debridement
• F Transforms wounds from inflammation phase to remodeling phase
• F As a scaffold for tissue regeneration

Indications :

• F Pressure ulcers
• F Venous stasis ulcers
• F Diabetic ulcers
• F Acute wounds for example trauma and surgical wounds
• F Partial thickness burns
• F Moderate to heavily exuding wounds

Contraindications :

• F Do not apply Kolspon® on infected wounds
• F In case of infection, control with systemic antibiotics and resume the application
• F In case of irritation, remove and discontinue Kolspon®
• F Do not apply on patients hypersensitive to collagen

Application Methodology :

• F Ensure wound bed is thoroughly cleansed
• F Select the required dimension of Kolspon® depending upon the size and depth wound
• F Kolspon® can be applied dry or moist depending upon the type of wound bed
• F Secure the sponge with a secondary dressing of choice
• F For early removal or change of Kolspon®, irrigate with normal saline

Do not pack the wound tightly sponge is highly absorbent and need room for expansion. Always maintain a moist wound environment.

Product Description : Hydrez®-Plus is a silver impregnated hydrophilic foam dressing with a transparent breathable Polyurethane skin and soft silicone wound contact layer. The silicone wound contact layer is highly perforated thereby enabling the routine vertical absorption of exudates by the foam and also protecting the fragile wound bed from being macerated. Hydrez®-Plus is offered with & without an adhesive border.

Salient Features :

• F Painless removal or re-positioning
• F High Fluid handling capacity
• F Adhesive border dressing prevents the need of secondary dressing or fixators
• F High Patient compliance
• F Can be kept in place up to 4 days

 

Indications :

• F Moderate to Highly exuding wounds
• F Diabetic Ulcers
• F Pressure sores & ulcers
• F Traumatic wounds
• F Incision sites
• F Venous stasis ulcers
• F Post-operative Surgical sites
• F Lacerations & abrasions

Contraindications :

• F Hydrez®-Plus is not be surgically implanted.
• F Do not use Hydrez®-Plus on patients with a known sensitivity to silver, polyurethane foams of silicone.

Application Methodology :

• Prepare the wound bed as per your standard protocol. An initial debarment of the wound may be essential to ensure
• that the wound edges contain viable tissue.
• Always maintain moist wound environment. Ensure that wound bed is thoroughly cleansed and is free of debris and
• necrotic tissue.
• Sterile technique should always be used to remove Hydrez®-Plus from its packaging.
• Remove the release film and make sure HydrezTM-Plus overlaps the wound bed by at-least 2cm onto the surrounding
• skin. Apply the silicone adherent side on the wound.
• If use of Hydrez®-Plus with an adhesive dressing, there is no need of a secondary dressing or else Hydrez®-Plus
• can be secured with suitable secondary dressing or fixator.
• Hydrez®-Plus can be applied up to 4 days or changed according to the wound condition or the clinician's discretion.

Precautions and Warnings :

•  Product for use by Registered Medical Practitioner or a Hospital.
• Hydrez®-Plus is supplied as a sterile product and is strictly for single use only. Do not re-sterilize as the process may
• result in change of product characteristics.
• Unused, opened packages of Hydrez®-Plus should be discarded to avoid cross contamination and hospital acquired
• infection on the device upon storage.
• Sterility of Hydrez®-Plus is not guaranteed when the unused portion of the device is left in the pack.
• Ensure the dressing is applied to the wound pink side up.
• Securing of Hydrez®-Plus with occlusive films or tapes is not recommended, as these reduce moisture vapor loss,
• which may impair the effectiveness of the dressing.

Be it online payment processing or offline payment processing, we are capable of executing both as per your convenience. We take care of all your transactions made; by this, we make all the procedures transparent. Designed and developed using the premium raw material and modern work methods; we guarantee high quality standards and longevity of our products. Also, we make sure that the raw material is sourced from the trusted places.

We offer Neuskin sterile collagen membrane in dry form the bovine collagen membrane is offered in freeze dried form to avoid pre-treatment of collagen membrane in normal saline before application. It is gamma sterilized and available in different dimensions. Neuskin - trade mark under registration in india.