Prescription Products

Medifil® II is Kollagen™ in particle form. The particles have a high surface area, allowing them to effectively penetrate and deliver the maximum amount of Kollagen™ into the wound surface. Medifil® II is 100% non-hydrolyzed type 1 bovine native collagen. Human BioSciences, Inc.’s proprietary Kollagen™ technology process protects and retains significantly more native triple helical protein structure, thus allowing superior stability of the molecule and scaffolding through all four phases of wound healing.

 

Dressing wear time should be based on the condition of the wound and clinical assessment. Always consult a physician for changes in wound condition and treatment plan monitoring and follow up.

  1. Cleanse wound as per physician order: preferably normal saline or non-cytotoxic wound cleanser or wash.
  2. Line wound bed with Medifil ® II collagen particles up to 1/4 inch depth.
  3. Cover wound with a secondary dressing: e.g. transparent, gauze, abdominal pad, foam, super absorbent pad, hydrocolloid to promote thermoregulation and enhance wound healing.

Partial-thickness wounds – Loss involving epidermis, dermis, or both. Shallow open ulcer. Red/pink wound bed, without slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 2
  • Blisters 
  • Second-degree burns
  • Superficial abrasions

 

Full thickness wounds – Loss of epidermis, dermis, into subcutaneous tissue or extending to muscle, tendon, and bone. Subcutaneous fat may or may not be visible. Slough and or eschar may or may not be present. *Collagen can be used in wounds with scattered slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 3,4
  • Donor sites
  • Dehisced surgical wounds
  • Traumatic wounds healing by secondary intention.
  • Do not use on third-degree (full thickness) burns.
  • Do not use on patients with collagen or bovine sensitivities.

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SkinTemp® II is Kollagen™ in sheet form. The dressings are porous collagen membranes which are designed to be permeable and breathable, with fluid control similar to skin. They are flexible, pliable, elastic, and durable for ease of application. SkinTemp® II is 100% non-hydrolyzed type 1 bovine native collagen. Human BioSciences, Inc.’s proprietary Kollagen™ technology process protects and retains significantly more native triple helical protein structure, thus allowing superior stability of the molecule and scaffolding through all four phases of wound healing. 

 

 

Dressing wear time should be based on the condition of the wound and clinical assessment. Always consult a physician for changes in wound condition and treatment plan monitoring and follow up.

  1. Cleanse wound as per physician order: preferably normal saline or a non-cytotoxic wound cleanser or wash.
  2. Remove Skin Temp® II backing from the collagen sheet.
  3. Apply Skin Temp® II collagen sheet to the wound bed. Place collagen sheet with white side down, to make direct contact with the wound bed.
  4. Skin Temp® II may be layered to fill dead space of deep cavity wounds and packed loosely into undermining and tunneling wounds.
  5. Rehydrate Skin Temp® II with normal saline in dry wounds.
  6. Cover wound with a secondary dressing: e.g. transparent, gauze, abdominal pad, foam, super absorbent pad, hydrocolloid to promote thermoregulation in wound healing.
  7. For removal, moisten dressing with normal saline to avoid harming new tissue and causing pain.

Partial-thickness wounds – Loss involving epidermis, dermis, or both. Shallow open ulcer. Red/pink wound bed, without slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 2
  • Blisters 
  • Second-degree burns
  • Superficial abrasions

 

Full thickness wounds – Loss of epidermis, dermis, into subcutaneous tissue or extending to muscle, tendon, and bone. Subcutaneous fat may or may not be visible. Slough and or eschar may or may not be present. *Collagen can be used in wounds with scattered slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 3,4
  • Donor sites
  • Dehisced surgical wounds
  • Traumatic wounds healing by secondary intention.
  • Do not use on patients with collagen or bovine sensitivities.
  • Do not use on third-degree (full thickness) burns.

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Collatek® Gel is collagen in a viscous gel form.  Collatek® is a sterile collagen gel that encourages healing by donating moisture to the wound. Wounds heal best in a moist wound environment. Collatek® Gel  can be used with our Medifil II collagen particles in hard to reach areas in wounds (tunneling and undermining). Collatek® Gel is beneficial for partial and full thickness wounds.

 
  1. Cleanse wound as per physician order. Preferably normal saline or non-cytotoxic wound cleanser or wash.
  2. Apply Collatek® Collagen Gel to the wound bed.
  3. Cover wound with a secondary dressing: e.g., transparent, gauze, abdominal pad, foam, super-absorbent, and/or hydrocolloid to promote thermoregulation in wound healing.
  4. Change dressing daily.

Partial-thickness wounds – Loss involving epidermis, dermis, or both. Shallow open ulcer. Red/pink wound bed, without slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 2
  • Blisters 
  • Second-degree burns
  • Superficial abrasions

 

Full thickness wounds – Loss of epidermis, dermis, into subcutaneous tissue or extending to muscle, tendon, and bone. Subcutaneous fat may or may not be visible. Slough and or eschar may or may not be present. *Collagen can be used in wounds with scattered slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 3,4
  • Donor sites
  • Dehisced surgical wounds
  • Traumatic wounds healing by secondary intention.
  • Do not use on patients with collagen or bovine sensitivities.
  • Do not use on third-degree (full thickness) burns.

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The Collatek foam dressing is a bi-layer dressing technology that consists of a collagen impregnated polyurethane foam designed to absorb minimal to heavy exudates, while promoting the wound microenvironment for faster healing.  Collatek foam dressings can be used in patients at risk for pressure injury.  They can be applied to vulnerable areas like the elbows and heels. 

 
  1. Cleanse wound as per physician order: preferably normal saline or non-cytotoxic wound cleanser or wash.
  2. Apply Collatek foam dressing making sure the dressing extends a minimum of one inch beyond the edges of the wound.
  3. For Non-border Collatek foam dressings, use tape or a wrap to secure the dressing depending on the location of the wound. 
  4. Collatek foam dressings should be changed depending on the exudate amount or if the dressing becomes soiled.

Partial-thickness wounds – Loss involving epidermis, dermis, or both. Shallow open ulcer. Red/pink wound bed, without slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 2
  • Blisters 
  • Second-degree burns
  • Superficial abrasions

 

Full thickness wounds – Loss of epidermis, dermis, into subcutaneous tissue or extending to muscle, tendon, and bone. Subcutaneous fat may or may not be visible. Slough and or eschar may or may not be present. *Collagen can be used in wounds with scattered slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 3,4
  • Donor sites
  • Dehisced surgical wounds
  • Traumatic wounds healing by secondary intention.
  • Do not use on patients with collagen or bovine sensitivities.
  • Do not use on third-degree (full thickness) burns and dry or non-draining wounds.

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The Collatek hydrocolloid dressing is a waterproof, self-adhesive dressing containing collagen to promote healing. Hydrocolloid dressings allow the wound to heal using its own enzymes. This provides a moist and insulating healing environment. The hydrocolloid’s conformable self-adhesive makes it easy to apply, even to traditionally difficult to dress areas such as elbows and heels.

 
  1. Cleanse wound as per physician order: preferably normal saline or non-cytotoxic wound cleanser or wash.
  2. The dressing should extend at least 2 cm beyond the wound margins.
  3. Peel off the backing carefully while pressing the pad gently on the skin. The warmth of the hand can be used for 20 seconds to help seal the dressing.
  4. The dressing should be changed every 3–7 days.

Partial-thickness wounds – Loss involving epidermis, dermis, or both. Shallow open ulcer. Red/pink wound bed, without slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 2
  • Blisters 
  • Second-degree burns
  • Superficial abrasions

 

Full thickness wounds – Loss of epidermis, dermis, into subcutaneous tissue or extending to muscle, tendon, and bone. Subcutaneous fat may or may not be visible. Slough and or eschar may or may not be present. *Collagen can be used in wounds with scattered slough or eschar.

  • Arterial Ulcers
  • Venous Leg Ulcers (VLUs)
  • Diabetic Foot Ulcers (DFUs)
  • Pressure Injury (PIs) Stage 3,4
  • Donor sites
  • Dehisced surgical wounds
  • Traumatic wounds healing by secondary intention.
  • Do not use it on patients with collagen or bovine sensitivities.
  • Do not use on third-degree (full thickness) burns or actively infected ulcers.
  • Require a secondary dressing.
  • Not recommended for necrotic wounds.
  • May require rehydration on removal.

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All of our proprietary Kollagen™ products are made of 100% native, non-hydrolyzed type I bovine hide collagen. Do not use any of these products if you have a known sensitivity to bovine collagen.