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합성 메쉬 Bard™ soft mesh

Bard™ Soft Mesh, Rectangle, 4 in x 6 in (10 cm x 15 cm)

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지원
Becton, Dickinson and Company
전화 아이콘
(82.2) 080-340-3800
bd_korea@bd.com
모달 닫기 아이콘
감사 모달 닫기 아이콘
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영업 담당자가 곧 연락을 드립니다.
Address
위치 아이콘
Becton Dickinson Korea Co., Ltd. 한국 서울특별시 강남구 테헤란로 142 아크플레이스 16층 06236
Overview
경량 메쉬

개복 및 복강경 탈장 수복을 위해 설계


Bard™ 소프트 메쉬는 유연성, 둥근 모서리, 그리고 절단 시 잘 풀리거나 마모되지 않는 대형 기공 니트 구조를 제공합니다. 임플란트의 재료를 줄이는 것을 선호하는 외과의의 경우, 기존의 폴리프로필렌 메쉬보다 약 60% 가벼우며*, 메쉬 배치를 용이하게 하는 부드럽고 얇은 니트 구조를 제공합니다.

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Features and Benefits
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Specification

GTIN - Case

10801741030878

3

GTIN - Each

00801741030871

1


Quantity

3/cs.


Dimensions

4" x 6" (10cm x 15cm)

GTIN

GTIN - Case 10801741030878 3
GTIN - Each 00801741030871 1

Packaging

Quantity 3/cs.

Product Basic Specification

Dimensions 4" x 6" (10cm x 15cm)
Electronic Instructions for Use (eIFUs)
Resources
Frequently Asked Questions
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Related Products
RELATED PRODUCTS NOT AVAILABLE
References

* As compared to other traditional polypropylene mesh, such as Classic Bard™ Mesh

INDICATIONS

BARD® Soft Mesh is indicated to reinforce soft tissue where weakness exists, e.g., repair of hernias and chest wall defects.

CONTRAINDICATIONS

Do not use Bard™ Soft Mesh in infants or children, in whom future growth will be compromised by use of such mesh material. Literature reports that there may be a possibility for adhesion formation when the polypropylene mesh is placed in direct contact with the bowel or viscera.

WARNINGS

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

Intact Bard™ Soft Mesh exhibits high burst and tensile strength. However, when custom tailoring, in special circumstances where excessive force is placed on the mesh, the following guidelines may be helpful:

When cutting a notch in the mesh, a V-shape with a radiused point will withstand more force than a V-shape which comes to a sharp point.

Davol™ permanent or absorbable fixation devices or nonabsorbable monofilament sutures are recommended to properly secure the prosthesis. If absorbable fixation devices are used, they must be indicated for use in hernia repair. Care should be taken to ensure that the mesh is adequately fixated to the uncompromised tissue of the inguinal floor. If necessary, additional fasteners and/or sutures should be used.

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.

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