Integra® 3724269

GUDID 10381780084402

Juers Crimper Forceps, Serrated Jaws Offset Left, Shaft 3"

INTEGRA LIFESCIENCES PRODUCTION CORPORATION

Surgical soft-tissue manipulation forceps, alligator, reusable

• Primary Device ID: 10381780084402
• NIH Device Record Key: caa52f5e-8afe-4689-a233-08ae3d3ec5a4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Integra®
• Version Model Number: 3724269
• Catalog Number: 3724269
• 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	10381780084402 [Primary]

FDA Product Code

• HYA: FORCEPS, WIRE HOLDING

Sterilization

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

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

Moist Heat or Steam Sterilization

[10381780084402]

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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