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Becton, Dickinson and Company
전화 아이콘
(82.2) 080-340-3800
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위치 아이콘
Becton Dickinson Korea Co., Ltd. 한국 서울특별시 강남구 테헤란로 142 아크플레이스 16층 06236

PerFix™ Plug

무장력 개복 서혜부 탈장 수복 기술에 사용하도록 설계된 플러그와 패치.

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개요

서혜부 탈장 수복을 위한 빠르고 간단한 복막전 언더레이 수정 기술

PerFix™ Plug는 무장력 복막전 수복 기술에 사용하기에 적합합니다. Bard™ PerFix™ Plug 는 다양한 크기와 모양의 결손 부위에 쉽게 맞도록 주름진 가장자리로 설계되어 있습니다. 모노필라멘트 폴리프로필렌 설계는 건강한 조직 내성장을 보장합니다.

true
특징 및 이점
효율적입니다
효율적입니다

25분 내로 전체 수술 가능2 최소 절개 필요 4~5cm 절개1 모든 국소 또는 경막외 마취 사용 가능 모든 유형의 서혜부 탈장 수용

효과적입니다

무장력 수복 기술 사용 보고된 재발률 0.15%1 만성 통증 발생률 0.5% 미만1

참고 자료

1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.

2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023

INDICATIONS

This product is indicated for the repair of groin hernia defects.

CONTRAINDICATIONS

Literature reports that there may be a possibility for adhesion formation when Perfix™ Plug or the Polypropylene mesh is placed in direct contact with the bowel or viscera.

Do not use the PerFix™ Plug in infants or children, whereby future growth will be compromised by use of such mesh material.

WARNINGS

The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. An unresolved infection may require removal of the device.

PRECAUTIONS

Monofilament sutures are recommended to properly secure the PerFix™ Plug

ADVERSE REACTIONS

Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, fistula formation and recurrence of the hernia or soft tissue defect.

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

BD-126373

true
참고 자료

1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.

2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023

INDICATIONS

This product is indicated for the repair of groin hernia defects.

CONTRAINDICATIONS

Literature reports that there may be a possibility for adhesion formation when Perfix™ Plug or the Polypropylene mesh is placed in direct contact with the bowel or viscera.

Do not use the PerFix™ Plug in infants or children, whereby future growth will be compromised by use of such mesh material.

WARNINGS

The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. An unresolved infection may require removal of the device.

PRECAUTIONS

Monofilament sutures are recommended to properly secure the PerFix™ Plug

ADVERSE REACTIONS

Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, fistula formation and recurrence of the hernia or soft tissue defect.

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

BD-126373

true
EIFU
리소스
참고 자료

1. Millikan KW, Doolas A. A Long-Term Evaluation of the Modified Mesh-Plug Hernioplasty in Over 2,000 Patients. Hernia. 2008 June; 12(3): 257-260.

2. Rutkow, I.M. : The Perfix plug repair for groin hernias. Surg Clinics of N. America, 2003; 83; 5: 1079-1098; 78; 6: 1007-1023

INDICATIONS

This product is indicated for the repair of groin hernia defects.

CONTRAINDICATIONS

Literature reports that there may be a possibility for adhesion formation when Perfix™ Plug or the Polypropylene mesh is placed in direct contact with the bowel or viscera.

Do not use the PerFix™ Plug in infants or children, whereby future growth will be compromised by use of such mesh material.

WARNINGS

The use of any permanent mesh or patch in a contaminated or infected wound could lead to fistula formation and/or extrusion of the mesh. If an infection develops, treat the infection aggressively. Consideration should be given regarding the need to remove the mesh. An unresolved infection may require removal of the device.

PRECAUTIONS

Monofilament sutures are recommended to properly secure the PerFix™ Plug

ADVERSE REACTIONS

Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, fistula formation and recurrence of the hernia or soft tissue defect.

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

BD-126373

true
자주 묻는 질문
false
true