Ventralight™ ST 메쉬에 사전 부착된 로우 프로파일 풍선이 있어 복강경 복부 탈장 수복 시 배치, 설치 및 위치 조정을 용이하게 합니다.
true
{"AlternateComparison":false,"RelatedProducts":false,"Specification":true,"FeatureBenefit":false}
Ventralight™
합성 메쉬
Ventralight™ ST Mesh with Echo PS™ Positioning System
![감사 모달 닫기 아이콘]()
Ventralight™ ST Mesh with Echo PS™ Positioning System, Ellipse, 10 in x 13 in (25.4 cm x 33.0 cm)
지원
Becton, Dickinson and Company
(82.2) 080-340-3800
bd_korea@bd.com
영업팀에 연락해 주셔서 감사합니다!
영업 담당자가 곧 연락을 드립니다.
Address
Becton Dickinson Korea Co., Ltd. 한국 서울특별시 강남구 테헤란로 142 아크플레이스 16층 06236
- Overview
- Specifications
- eIFUs and Resources
- FAQ
true
FEATURE AND BENEFIT CARDS NOT AVAILABLE
FEATURE AND BENEFIT CARDS NOT AVAILABLE
GTIN - Case
00801741031694
1
Quantity
1/cs
Dimensions
10” x 13” (25.4cm x 33cm) Ellipse
GTIN
| GTIN - Case | 00801741031694 | 1 |
Packaging
| Quantity | 1/cs |
Product Basic Specification
| Dimensions | 10” x 13” (25.4cm x 33cm) Ellipse |
false
1 When compared to positioning with transfascial sutures in a preclinical study.
Date on file at C. R. Bard, Inc. Results may not correlate to performance in humans.
INDICATIONS
Ventralight™ ST Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias. Composix™ L/P Mesh is indicated for use in the reconstruction of soft tissue deficiencies, such as for the repair of hernias and chest wall defects. The Echo PS™ Positioning System is intended to be used to facilitate the delivery of soft tissue prostheses during laparoscopic hernia repair.
CONTRAINDICATIONS
Literature reports there is a possibility for adhesion formation when the polypropylene is placed in direct contact with the bowel or viscera.
WARNINGS
Ventralight™ ST Mesh/Composix™ L/P Mesh is the only permanent implant component of the device. The inflation adapter and syringe are to be kept external to the patient and discarded after use. The Echo PS™ Positioning System (including the balloon, all connectors, and inflation tube) is to be removed from the patient and appropriately discarded as it is not part of the permanent implant.
The Echo PS™ Positioning System should not be used with any other hernia prosthesis aside from those with which it comes pre-attached/packaged.
PRECAUTIONS
Do not trim the mesh. This will affect the interface between the mesh and positioning system.
ADVERSE REACTIONS
Possible complications include seroma, adhesions, hematomas, inflammation, extrusion, fistula formation, infection, allergic reaction, 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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