Icon to close the modal
지원
Becton, Dickinson and Company
전화 아이콘
(82.2) 080-340-3800
bd_korea@bd.com
모달 닫기 아이콘
감사 모달 닫기 아이콘
영업팀에 연락해 주셔서 감사합니다!
영업 담당자가 곧 연락을 드립니다.
Address
위치 아이콘
Becton Dickinson Korea Co., Ltd. 한국 서울특별시 강남구 테헤란로 142 아크플레이스 16층 06236

Avitene™ Ultrafoam™ Collagen Sponge

Ultrafoam™ 콜라겐 스폰지

당사로 문의하기
Background Image
로딩
개요

지혈에 대해 검증된 솔루션으로 표준화하십시오.

Avitene™ 미세원섬유 콜라겐 기반 지혈제는 혈전 형성을 가속화하는 것으로 입증된 활성 흡수성 콜라겐 지혈제입니다. Avitene™은 혈소판 응집과 단백질 방출을 효과적으로 촉진해 섬유소를 형성하여 지혈합니다.

true
특징 및 이점

각 분야에 맞는 다양한 형태 제공:

  • 신경외과 포함 모든 수술 분야 출혈 제어에 입증된 솔루션
  • 40년 이상 받아온 안전성 및 유효성에 대한 외과의들의 신뢰
Avitene™ 시트

Avitene™ 시트

  • 어떤 모양이나 크기로든 절단 가능
  • 평평한 표면이나 혈관 및 문합 부위를 감싸기에 적합
  • 자세히 알아보기
Avitene™ Ultrafoam™ 콜라겐 스폰지

Avitene™ Ultrafoam™ 콜라겐 스폰지

  • 지혈을 위한 쉽고 효과적인 솔루션
  • 동물 연구에서 트롬빈이 없는 UltraFoam™ 콜라겐은 트롬빈이 있는 G 스폰지만큼 효과적
  • 트롬빈 사용 감소로 비용 절감 가능
  • 부드럽고 유연한 스폰지는 개봉 후 바로 사용 가능하며 , 담그는 과정
    불필요

관련 제품

참고 자료

Please note, not all products, services or features of products and services may be available in your local area. Please check with your local BD representative.

Animal data may not correlate to outcomes in humans. Data on file.

Indications

Avitene™ Microfibrillar Collagen Hemostat (MCH) and Avitene™ UltraFoam™ sponge are indicated in surgical procedures as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

Contraindications

•Avitene™ MCH and Avitene™ UltraFoam™ sponge should not be used in the closure of skin incisions as they may interfere with the healing of the skin edges. This is due to simple mechanical interposition of dry collagen and not to any intrinsic interference with wound healing.

•It has been reported with other collagen hemostatic agents, that by filling porosities of cancellous bone, they may significantly reduce the bond strength of methylmethacrylate adhesives. Avitene™ MCH and Avitene™ UltraFoam™ sponge should not, therefore, be employed on bone surfaces to which prosthetic materials are to be attached with methylmethacrylate adhesives.

 

Warnings

•Avitene™ MCH and Avitene™ UltraFoam™ are inactivated by autoclaving. Ethylene oxide reacts with bound hydrochloric acid to form ethylene chlorohydrin. These devices have been designed for single use only. Reuse, reprocessing, resterilization or repackaging may compromise the structural integrity and/or essential material and design characteristics that are critical to the overall performance of the devices and may lead to device failure which may result in injury to the patient. Reuse, reprocessing, resterilization or repackaging may also create a risk of contamination of the device and/or cause patient infection or cross infection, including, but not limited to, the transmission of infectious diseases from one patient to another. Contamination of the devices may lead to injury, illness or death of the patient or end user. Opened, unused product should be discarded. Moistening Avitene™ MCH or wetting with saline or thrombin impairs its hemostatic efficacy. It should be used dry.

•As with any foreign substance, use of Avitene™ MCH and Avitene™ UltraFoam™ in contaminated wounds may enhance infection.

•Avitene™ UltraFoam™ sponge should not be used in instances of pumping arterial hemorrhage.

•Avitene™ UltraFoam™ should not be used where blood or other fluids have pooled, or in cases where the point of hemorrhage is submerged as it may mask an underlying source of bleeding, resulting in hematoma.

•Avitene™ UltraFoam™ sponge will not act as a tampon or plug in a bleeding site, nor will it close off an area of blood collecting behind a tampon.

•Avitene™ UltraFoam™ sponge is not intended to treat systemic coagulation disorders. Avitene™ MCH and Avitene™ UltraFoam™ are not for injection, intraocular or intravascular use.

 

Adverse Reactions

•The most serious adverse reaction reported which may be related to the use of Avitene™ MCH or other collagen products are potentiation of infection including abscess formation, hematoma, wound dehiscence and mediastinitis.

•Other reported adverse reactions possibly related are adhesion formation, allergic reaction, foreign body reaction and subgaleal seroma (report of a single case) and increased incidence of alveolalgia when used for packing of dental extraction sockets.

•Transient laryngospasm due to aspiration of dry material has been reported following use of Avitene™ MCH in tonsillectomy.

Please consult package insert for more detailed safety information and instructions for use.

References

See full Instructions for Use for detailed application instructions.

true

관련 제품

참고 자료

Please note, not all products, services or features of products and services may be available in your local area. Please check with your local BD representative.

Animal data may not correlate to outcomes in humans. Data on file.

Indications

Avitene™ Microfibrillar Collagen Hemostat (MCH) and Avitene™ UltraFoam™ sponge are indicated in surgical procedures as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

Contraindications

•Avitene™ MCH and Avitene™ UltraFoam™ sponge should not be used in the closure of skin incisions as they may interfere with the healing of the skin edges. This is due to simple mechanical interposition of dry collagen and not to any intrinsic interference with wound healing.

•It has been reported with other collagen hemostatic agents, that by filling porosities of cancellous bone, they may significantly reduce the bond strength of methylmethacrylate adhesives. Avitene™ MCH and Avitene™ UltraFoam™ sponge should not, therefore, be employed on bone surfaces to which prosthetic materials are to be attached with methylmethacrylate adhesives.

 

Warnings

•Avitene™ MCH and Avitene™ UltraFoam™ are inactivated by autoclaving. Ethylene oxide reacts with bound hydrochloric acid to form ethylene chlorohydrin. These devices have been designed for single use only. Reuse, reprocessing, resterilization or repackaging may compromise the structural integrity and/or essential material and design characteristics that are critical to the overall performance of the devices and may lead to device failure which may result in injury to the patient. Reuse, reprocessing, resterilization or repackaging may also create a risk of contamination of the device and/or cause patient infection or cross infection, including, but not limited to, the transmission of infectious diseases from one patient to another. Contamination of the devices may lead to injury, illness or death of the patient or end user. Opened, unused product should be discarded. Moistening Avitene™ MCH or wetting with saline or thrombin impairs its hemostatic efficacy. It should be used dry.

•As with any foreign substance, use of Avitene™ MCH and Avitene™ UltraFoam™ in contaminated wounds may enhance infection.

•Avitene™ UltraFoam™ sponge should not be used in instances of pumping arterial hemorrhage.

•Avitene™ UltraFoam™ should not be used where blood or other fluids have pooled, or in cases where the point of hemorrhage is submerged as it may mask an underlying source of bleeding, resulting in hematoma.

•Avitene™ UltraFoam™ sponge will not act as a tampon or plug in a bleeding site, nor will it close off an area of blood collecting behind a tampon.

•Avitene™ UltraFoam™ sponge is not intended to treat systemic coagulation disorders. Avitene™ MCH and Avitene™ UltraFoam™ are not for injection, intraocular or intravascular use.

 

Adverse Reactions

•The most serious adverse reaction reported which may be related to the use of Avitene™ MCH or other collagen products are potentiation of infection including abscess formation, hematoma, wound dehiscence and mediastinitis.

•Other reported adverse reactions possibly related are adhesion formation, allergic reaction, foreign body reaction and subgaleal seroma (report of a single case) and increased incidence of alveolalgia when used for packing of dental extraction sockets.

•Transient laryngospasm due to aspiration of dry material has been reported following use of Avitene™ MCH in tonsillectomy.

Please consult package insert for more detailed safety information and instructions for use.

References

See full Instructions for Use for detailed application instructions.

true
EIFU
리소스
참고 자료

Please note, not all products, services or features of products and services may be available in your local area. Please check with your local BD representative.

Animal data may not correlate to outcomes in humans. Data on file.

Indications

Avitene™ Microfibrillar Collagen Hemostat (MCH) and Avitene™ UltraFoam™ sponge are indicated in surgical procedures as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical.

Contraindications

•Avitene™ MCH and Avitene™ UltraFoam™ sponge should not be used in the closure of skin incisions as they may interfere with the healing of the skin edges. This is due to simple mechanical interposition of dry collagen and not to any intrinsic interference with wound healing.

•It has been reported with other collagen hemostatic agents, that by filling porosities of cancellous bone, they may significantly reduce the bond strength of methylmethacrylate adhesives. Avitene™ MCH and Avitene™ UltraFoam™ sponge should not, therefore, be employed on bone surfaces to which prosthetic materials are to be attached with methylmethacrylate adhesives.

 

Warnings

•Avitene™ MCH and Avitene™ UltraFoam™ are inactivated by autoclaving. Ethylene oxide reacts with bound hydrochloric acid to form ethylene chlorohydrin. These devices have been designed for single use only. Reuse, reprocessing, resterilization or repackaging may compromise the structural integrity and/or essential material and design characteristics that are critical to the overall performance of the devices and may lead to device failure which may result in injury to the patient. Reuse, reprocessing, resterilization or repackaging may also create a risk of contamination of the device and/or cause patient infection or cross infection, including, but not limited to, the transmission of infectious diseases from one patient to another. Contamination of the devices may lead to injury, illness or death of the patient or end user. Opened, unused product should be discarded. Moistening Avitene™ MCH or wetting with saline or thrombin impairs its hemostatic efficacy. It should be used dry.

•As with any foreign substance, use of Avitene™ MCH and Avitene™ UltraFoam™ in contaminated wounds may enhance infection.

•Avitene™ UltraFoam™ sponge should not be used in instances of pumping arterial hemorrhage.

•Avitene™ UltraFoam™ should not be used where blood or other fluids have pooled, or in cases where the point of hemorrhage is submerged as it may mask an underlying source of bleeding, resulting in hematoma.

•Avitene™ UltraFoam™ sponge will not act as a tampon or plug in a bleeding site, nor will it close off an area of blood collecting behind a tampon.

•Avitene™ UltraFoam™ sponge is not intended to treat systemic coagulation disorders. Avitene™ MCH and Avitene™ UltraFoam™ are not for injection, intraocular or intravascular use.

 

Adverse Reactions

•The most serious adverse reaction reported which may be related to the use of Avitene™ MCH or other collagen products are potentiation of infection including abscess formation, hematoma, wound dehiscence and mediastinitis.

•Other reported adverse reactions possibly related are adhesion formation, allergic reaction, foreign body reaction and subgaleal seroma (report of a single case) and increased incidence of alveolalgia when used for packing of dental extraction sockets.

•Transient laryngospasm due to aspiration of dry material has been reported following use of Avitene™ MCH in tonsillectomy.

Please consult package insert for more detailed safety information and instructions for use.

References

See full Instructions for Use for detailed application instructions.

true
true