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PerFix™ Synthetic mesh PerFix™ Light Plug

Bard® メッシュ (ライト パーフィックス® プラグ), Mサイズ, 3.3 cm x 3.9 cm

Overview
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Features and Benefits
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References

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.

INDICATIONS

The PerFix™ Light Plug is indicated for reinforcement of soft tissue, where weakness exists, in procedures involving soft tissue repair, such as groin hernia defects.

CONTRAINDICATIONS

Literature reports that there may be a possibility for adhesion formation when polypropylene mesh is placed in direct contact with the bowel or viscera. Do not use the PerFix™ Light 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™Light Plug

ADVERSE REACTIONS

Possible complications include seroma, adhesions, hematoma, inflammation, extrusion, infection, pain, mesh migration, 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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Specification

GTIN - Case

00801741030956

1


寸法

Mサイズ, 3.3 cm x 3.9 cm

数量

2入


販売名

Bard メッシュ

承認/認証/届出番号

16000BZY01128000

製造販売元

株式会社メディコン

GTIN

GTIN - Case 00801741030956 1

梱包

寸法 Mサイズ, 3.3 cm x 3.9 cm
数量 2入

薬事・その他情報

販売名 Bard メッシュ
承認/認証/届出番号 16000BZY01128000
製造販売元 株式会社メディコン
References
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Resources
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Frequently Asked Questions
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References
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Related Products
RELATED PRODUCTS NOT AVAILABLE
References
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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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Recall Notifications
These recall notices provide current information on medical device recalls.
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References
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