Integra® 3724063

GUDID 10381780083139

House Gelfoam Press, 16mm x 12mm Plate, 5-1/4" Long

INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Surgical soft-tissue manipulation forceps, scissors-like, reusable

• Primary Device ID: 10381780083139
• NIH Device Record Key: 416e7826-a01e-4f27-8479-b5cd022d0c88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integra®
• Version Model Number: 3724063
• Catalog Number: 3724063
• Company DUNS: 081277700
• Company Name: INTEGRA LIFESCIENCES PRODUCTION CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com
• Phone: +1(800)654-2873
• Email: custsvcnj@integralife.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10381780083139 [Primary]

FDA Product Code

• JYW: PRESS, VEIN

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

[10381780083139]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-05
• Device Publish Date: 2018-10-24

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